Linked Data
dbSNP Id:
rs3819276
ExAC:
6:31323027 C / T
gnomAD v2:
6-31323027-C-T
gnomAD v3:
6-31355250-C-T
gnomAD v4:
6-31355250-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31355250C>T , CM000668.2:g.31355250C>T | GRCh38 |
| NC_000006.11:g.31323027C>T , CM000668.1:g.31323027C>T | GRCh37 |
| NC_000006.10:g.31431006C>T | NCBI36 |
| NG_023187.1:g.6963G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000474381.2:n.2943-27G>A (HLA-B) | ||
| ENST00000481849.6:n.2435G>A (HLA-B) | ||
| ENST00000497377.6:n.2369-27G>A (HLA-B) | ||
| ENST00000640094.2:c.895+67G>A (HLA-B) | ENSP00000491275.2:n.895+67G>A | |
| ENST00000696558.1:c.965-27G>A (HLA-B) | ENSP00000512716.1:n.965-27G>A | |
| ENST00000696559.1:c.896-27G>A (HLA-B) | ENSP00000512717.1:n.896-27G>A | |
| ENST00000696560.1:c.896-27G>A (HLA-B) | ENSP00000512718.1:n.896-27G>A | |
| ENST00000696561.1:c.896-27G>A (HLA-B) | ENSP00000512719.1:n.896-27G>A | |
| ENST00000696562.1:c.896-27G>A (HLA-B) | ENSP00000512720.1:n.896-27G>A | |
| ENST00000412585.7:c.896-27G>A (HLA-B) MANE Select | ENSP00000399168.2:n.896-27G>A | |
| ENST00000640094.1:c.88+67G>A (HLA-B) | ENSP00000491275.1:n.88+67G>A | |
| ENST00000412585.6:c.896-27G>A (HLA-B) | ENSP00000399168.2:n.896-27G>A | |
| ENST00000463574.1:n.487-27G>A (HLA-B) | ||
| NM_005514.6:c.896-27G>A (HLA-B) | NP_005505.2:n.896-27G>A | |
| NR_106951.1:n.67G>A (MIR6891) | ||
| XM_011514556.1:c.929-27G>A (HLA-B) | XP_011512858.1:n.929-27G>A | |
| XM_011514557.1:c.895+67G>A (HLA-B) | XP_011512859.1:n.895+67G>A | |
| XR_926175.1:n.1335-27G>A (HLA-B) | ||
| NM_005514.7:c.896-27G>A (HLA-B) | NP_005505.2:n.896-27G>A | |
| NM_005514.8:c.896-27G>A (HLA-B) MANE Select | NP_005505.2:n.896-27G>A |