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HLA > Allele Frequency Search > Classical |
Please specify your search by selecting options from boxes. Then, click "Search" to find HLA allele frequencies
that match your criteria. Remember at least one option must be selected.
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Note: The aim of this search option is to display frequencies organised by population. If your selected criteria retrieves alleles that have been found in more than one hundred populations the number of columns will be limited. For a best view please reduce the number of populations to compare.
| Line | Allele |
| ||
|---|---|---|---|---|
| Allele Freq | ||||
| 1 | A*01:01 | 0.123 | ||
| 2 | A*01:06 | 0.000 | ||
| 3 | A*02:01 | 0.019 | ||
| 4 | A*02:03 | 0.037 | ||
| 5 | A*02:11 | 0.086 | ||
| 6 | A*02:22 | 0.000 | ||
| 7 | A*02:24 | 0.000 | ||
| 8 | A*02:36 | 0.012 | ||
| 9 | A*03:01:01 | 0.093 | ||
| 10 | A*03:01:02 | 0.000 | ||
| 11 | A*03:02 | 0.000 | ||
| 12 | A*11:01 | 0.123 | ||
| 13 | A*11:02 | 0.000 | ||
| 14 | A*23:04 | 0.000 | ||
| 15 | A*24:02 | 0.167 | ||
| 16 | A*24:03 | 0.000 | ||
| 17 | A*24:05 | 0.000 | ||
| 18 | A*24:06 | 0.025 | ||
| 19 | A*24:07 | 0.037 | ||
| 20 | A*24:08 | 0.000 | ||
| 21 | A*24:24 | 0.000 | ||
| 22 | A*25:01 | 0.000 | ||
| 23 | A*26:01 | 0.000 | ||
| 24 | A*26:08 | 0.000 | ||
| 25 | A*26:11N | 0.000 | ||
| 26 | A*26:14 | 0.000 | ||
| 27 | A*29:01 | 0.000 | ||
| 28 | A*29:02 | 0.000 | ||
| 29 | A*30:01 | 0.000 | ||
| 30 | A*31:01:02 | 0.043 | ||
| 31 | A*31:08 | 0.000 | ||
| 32 | A*32:01 | 0.006 | ||
| 33 | A*32:04 | 0.000 | ||
| 34 | A*33:01 | 0.000 | ||
| 35 | A*33:03 | 0.130 | ||
| 36 | A*36:01 | 0.000 | ||
| 37 | A*66:01 | 0.025 | ||
| 38 | A*68:01:01 | 0.019 | ||
| 39 | A*68:01:02 | 0.056 | ||
| 40 | A*68:03 | 0.000 | ||
| 41 | A*68:09 | 0.000 | ||
| 42 | A*68:11N | 0.000 | ||
| 43 | A*74:04 | 0.000 | ||
| Totals | 1.001 | |||
| Number of Alleles (k) | 0 | |||
| Heterozygosity (h) | 0.0000 | |||
| 44 | B*07:02 | 0.049 | ||
| 45 | B*07:04 | 0.000 | ||
| 46 | B*07:05 | 0.086 | ||
| 47 | B*07:07 | 0.000 | ||
| 48 | B*08:01 | 0.000 | ||
| 49 | B*08:04 | 0.019 | ||
| 50 | B*08:05 | 0.000 | ||
| 51 | B*13:01 | 0.000 | ||
| 52 | B*13:02 | 0.043 | ||
| 53 | B*13:04 | 0.000 | ||
| 54 | B*14:01 | 0.000 | ||
| 55 | B*14:05 | 0.000 | ||
| 56 | B*15:01 | 0.000 | ||
| 57 | B*15:02 | 0.019 | ||
| 58 | B*15:03 | 0.000 | ||
| 59 | B*15:04 | 0.000 | ||
| 60 | B*15:09 | 0.000 | ||
| 61 | B*15:10 | 0.000 | ||
| 62 | B*15:17 | 0.000 | ||
| 63 | B*15:18 | 0.037 | ||
| 64 | B*15:36 | 0.000 | ||
| 65 | B*15:37 | 0.000 | ||
| 66 | B*18:01 | 0.019 | ||
| 67 | B*18:07 | 0.000 | ||
| 68 | B*27:04 | 0.025 | ||
| 69 | B*27:05 | 0.000 | ||
| 70 | B*27:08 | 0.012 | ||
| 71 | B*35:01 | 0.000 | ||
| 72 | B*35:03 | 0.056 | ||
| 73 | B*35:06 | 0.000 | ||
| 74 | B*35:10 | 0.000 | ||
| 75 | B*35:12 | 0.000 | ||
| 76 | B*35:15 | 0.000 | ||
| 77 | B*35:16 | 0.000 | ||
| 78 | B*35:17 | 0.000 | ||
| 79 | B*35:20 | 0.037 | ||
| 80 | B*35:25 | 0.000 | ||
| 81 | B*37:01 | 0.012 | ||
| 82 | B*38:02 | 0.012 | ||
| 83 | B*40:01 | 0.000 | ||
| 84 | B*40:05 | 0.000 | ||
| 85 | B*40:06 | 0.179 | ||
| 86 | B*40:11 | 0.000 | ||
| 87 | B*40:12 | 0.000 | ||
| 88 | B*44:03 | 0.000 | ||
| 89 | B*44:04 | 0.000 | ||
| 90 | B*44:06 | 0.105 | ||
| 91 | B*44:07 | 0.043 | ||
| 92 | B*44:08 | 0.000 | ||
| 93 | B*44:09 | 0.000 | ||
| 94 | B*48:02 | 0.000 | ||
| 95 | B*51:01:01 | 0.068 | ||
| 96 | B*51:01:02 | 0.000 | ||
| 97 | B*51:03 | 0.000 | ||
| 98 | B*51:06 | 0.000 | ||
| 99 | B*51:07 | 0.000 | ||
| 100 | B*51:10 | 0.000 | ||
| 101 | B*51:15 | 0.000 | ||
| 102 | B*52:01:01 | 0.056 | ||
| 103 | B*53:01 | 0.019 | ||
| 104 | B*53:03 | 0.000 | ||
| 105 | B*54:01 | 0.006 | ||
| 106 | B*55:01 | 0.000 | ||
| 107 | B*55:04 | 0.000 | ||
| 108 | B*56:01 | 0.000 | ||
| 109 | B*56:03 | 0.000 | ||
| 110 | B*56:04 | 0.000 | ||
| 111 | B*56:05 | 0.019 | ||
| 112 | B*58:01 | 0.074 | ||
| 113 | B*78:03 | 0.006 | ||
| Totals | 1.001 | |||
| Number of Alleles (k) | 0 | |||
| Heterozygosity (h) | 0.0000 | |||
| 114 | C*01:02 | 0.019 | ||
| 115 | C*01:04 | 0.006 | ||
| 116 | C*02:02:01 | 0.049 | ||
| 117 | C*02:03 | 0.006 | ||
| 118 | C*03:02 | 0.000 | ||
| 119 | C*03:03 | 0.080 | ||
| 120 | C*03:04:02 | 0.000 | ||
| 121 | C*03:06 | 0.000 | ||
| 122 | C*04:01 | 0.154 | ||
| 123 | C*04:01:02 | 0.000 | ||
| 124 | C*04:03 | 0.000 | ||
| 125 | C*04:04 | 0.000 | ||
| 126 | C*04:07 | 0.000 | ||
| 127 | C*05:01 | 0.000 | ||
| 128 | C*06:02 | 0.222 | ||
| 129 | C*06:03 | 0.000 | ||
| 130 | C*07:01:01 | 0.037 | ||
| 131 | C*07:02 | 0.086 | ||
| 132 | C*07:03 | 0.000 | ||
| 133 | C*07:04 | 0.099 | ||
| 134 | C*07:05 | 0.000 | ||
| 135 | C*07:07 | 0.006 | ||
| 136 | C*07:08 | 0.000 | ||
| 137 | C*07:14 | 0.000 | ||
| 138 | C*08:06 | 0.000 | ||
| 139 | C*12:02:01 | 0.056 | ||
| 140 | C*12:02:03 | 0.000 | ||
| 141 | C*12:04:01 | 0.000 | ||
| 142 | C*14:02:01 | 0.006 | ||
| 143 | C*14:03 | 0.000 | ||
| 144 | C*14:04 | 0.000 | ||
| 145 | C*15:02:01 | 0.086 | ||
| 146 | C*15:03 | 0.000 | ||
| 147 | C*15:07 | 0.006 | ||
| 148 | C*15:08 | 0.000 | ||
| 149 | C*16:01 | 0.037 | ||
| 150 | C*18:01 | 0.043 | ||
| Totals | 0.998 | |||
| Number of Alleles (k) | 0 | |||
| Heterozygosity (h) | 0.0000 | |||
| 151 | DQB1*02:01:01 | 0.081 | ||
| 152 | DQB1*02:02 | 0.120 | ||
| 153 | DQB1*03:01:01 | 0.136 | ||
| 154 | DQB1*03:01:03 | 0.000 | ||
| 155 | DQB1*03:02:01 | 0.027 | ||
| 156 | DQB1*03:03:02 | 0.039 | ||
| 157 | DQB1*04:01 | 0.027 | ||
| 158 | DQB1*04:02 | 0.004 | ||
| 159 | DQB1*05:01:01 | 0.116 | ||
| 160 | DQB1*05:02:01 | 0.004 | ||
| 161 | DQB1*05:03:01 | 0.089 | ||
| 162 | DQB1*06:01:01 | 0.283 | ||
| 163 | DQB1*06:01:02 | 0.031 | ||
| 164 | DQB1*06:02 | 0.019 | ||
| 165 | DQB1*06:03:01 | 0.004 | ||
| Totals | 0.980 | |||
| Number of Alleles (k) | 0 | |||
| Heterozygosity (h) | 0.0000 | |||
| 166 | DRB1*01:01:01 | 0.027 | ||
| 167 | DRB1*03:01:01 | 0.074 | ||
| 168 | DRB1*03:01:02 | 0.016 | ||
| 169 | DRB1*03:02:02 | 0.004 | ||
| 170 | DRB1*04:01:01 | 0.074 | ||
| 171 | DRB1*04:01:03 | 0.004 | ||
| 172 | DRB1*04:03:01 | 0.012 | ||
| 173 | DRB1*04:07:01 | 0.008 | ||
| 174 | DRB1*07:01:01 | 0.120 | ||
| 175 | DRB1*07:06 | 0.004 | ||
| 176 | DRB1*08:01:01 | 0.016 | ||
| 177 | DRB1*09:01:02 | 0.008 | ||
| 178 | DRB1*09:02 | 0.000 | ||
| 179 | DRB1*10:01:01 | 0.085 | ||
| 180 | DRB1*11:01:01 | 0.066 | ||
| 181 | DRB1*12:02:01 | 0.008 | ||
| 182 | DRB1*13:01:01 | 0.081 | ||
| 183 | DRB1*13:01:02 | 0.016 | ||
| 184 | DRB1*13:02:01 | 0.008 | ||
| 185 | DRB1*13:07:01 | 0.004 | ||
| 186 | DRB1*14:01:01 | 0.074 | ||
| 187 | DRB1*14:03:01 | 0.012 | ||
| 188 | DRB1*14:04 | 0.027 | ||
| 189 | DRB1*14:05:01 | 0.004 | ||
| 190 | DRB1*15:01:01 | 0.194 | ||
| 191 | DRB1*15:01:06 | 0.004 | ||
| 192 | DRB1*15:02:02 | 0.008 | ||
| 193 | DRB1*16:01:01 | 0.019 | ||
| Totals | 0.977 | |||
| Number of Alleles (k) | 28 | |||
| Heterozygosity (h) | 0.9151 | |||
Allele frequency net database (AFND) 2020 update: gold-standard data classification, open access genotype data and new query tools
Gonzalez-Galarza FF, McCabe A, Santos EJ, Jones J, Takeshita LY, Ortega-Rivera ND, Del Cid-Pavon GM, Ramsbottom K, Ghattaoraya GS, Alfirevic A, Middleton D and Jones AR Nucleic Acid Research 2020, 48:D783-8.
Liverpool, U.K.
support@allelefrequencies.net