dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31362069G>C , CM000668.2:g.31362069G>C | GRCh38 |
| NC_000006.11:g.31329846G>C , CM000668.1:g.31329846G>C | GRCh37 |
| NC_000006.10:g.31437825G>C | NCBI36 |
| NG_023187.1:g.144C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.1270+3674C>G (HLA-B) | ||
| ENST00000481849.6:n.1270+3674C>G (HLA-B) | ||
| ENST00000497377.6:n.1270+3674C>G (HLA-B) | ||
| ENST00000696559.1:c.-204+3674C>G (HLA-B) | ENSP00000512717.1:n.-204+3674C>G | |
| ENST00000696560.1:c.-204+3674C>G (HLA-B) | ENSP00000512718.1:n.-204+3674C>G | |
| ENST00000696561.1:c.-204+850C>G (HLA-B) | ENSP00000512719.1:n.-204+850C>G | |
| ENST00000696562.1:c.-136+3674C>G (HLA-B) | ENSP00000512720.1:n.-136+3674C>G | |
| ENST00000696690.1:n.2558C>G (DHFRP2) | ||
| ENST00000696691.1:n.3180C>G (DHFRP2) |