Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29792577C= , CM000668.2:g.29792577C= | GRCh38 |
| NC_000006.11:g.29760354C= , CM000668.1:g.29760354C= | GRCh37 |
| NC_000006.10:g.29868333C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000418983.1:n.174G= (HCG4) | ||
| ENST00000429037.2:n.213C= (HLA-V) | ||
| ENST00000446817.1:n.323C= (HLA-V) | ||
| ENST00000457107.5:n.224C= (HLA-V) | ||
| ENST00000476601.5:n.541C= (HLA-V) | ||
| NM_001207043.1:c.439C= | NP_001193972.1:p.Arg147= | |
| NR_002139.2:n.497G= (HCG4) | ||
| NR_132323.1:n.541C= |