gnomAD v2:
gnomAD v3:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31355253T>C , CM000668.2:g.31355253T>C | GRCh38 |
| NC_000006.11:g.31323030T>C , CM000668.1:g.31323030T>C | GRCh37 |
| NC_000006.10:g.31431009T>C | NCBI36 |
| NG_023187.1:g.6960A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.2943-30A>G (HLA-B) | ||
| ENST00000481849.6:n.2432A>G (HLA-B) | ||
| ENST00000497377.6:n.2369-30A>G (HLA-B) | ||
| ENST00000640094.2:c.895+64A>G (HLA-B) | ENSP00000491275.2:n.895+64A>G | |
| ENST00000696558.1:c.965-30A>G (HLA-B) | ENSP00000512716.1:n.965-30A>G | |
| ENST00000696559.1:c.896-30A>G (HLA-B) | ENSP00000512717.1:n.896-30A>G | |
| ENST00000696560.1:c.896-30A>G (HLA-B) | ENSP00000512718.1:n.896-30A>G | |
| ENST00000696561.1:c.896-30A>G (HLA-B) | ENSP00000512719.1:n.896-30A>G | |
| ENST00000696562.1:c.896-30A>G (HLA-B) | ENSP00000512720.1:n.896-30A>G | |
| ENST00000412585.7:c.896-30A>G (HLA-B) MANE Select | ENSP00000399168.2:n.896-30A>G | |
| ENST00000640094.1:c.88+64A>G (HLA-B) | ENSP00000491275.1:n.88+64A>G | |
| ENST00000412585.6:c.896-30A>G (HLA-B) | ENSP00000399168.2:n.896-30A>G | |
| ENST00000463574.1:n.487-30A>G (HLA-B) | ||
| NM_005514.6:c.896-30A>G (HLA-B) | NP_005505.2:n.896-30A>G | |
| NR_106951.1:n.64A>G (MIR6891) | ||
| XM_011514556.1:c.929-30A>G (HLA-B) | XP_011512858.1:n.929-30A>G | |
| XM_011514557.1:c.895+64A>G (HLA-B) | XP_011512859.1:n.895+64A>G | |
| XR_926175.1:n.1335-30A>G (HLA-B) | ||
| NM_005514.7:c.896-30A>G (HLA-B) | NP_005505.2:n.896-30A>G | |
| NM_005514.8:c.896-30A>G (HLA-B) MANE Select | NP_005505.2:n.896-30A>G |