Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186085794T>A , CM000666.2:g.186085794T>A | GRCh38 |
| NC_000004.11:g.187006948T>A , CM000666.1:g.187006948T>A | GRCh37 |
| NC_000004.10:g.187243942T>A | NCBI36 |
| NG_007278.1:g.21640T>A , LRG_117:g.21640T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698352.1:c.*3188T>A | ENSP00000513675.1:n.*3188T>A | |
| ENST00000698353.1:n.3511T>A | ||
| ENST00000698354.1:c.*921T>A | ENSP00000513676.1:n.*921T>A | |
| ENST00000296795.8:c.*921T>A MANE Select | ENSP00000296795.3:n.*921T>A | |
| ENST00000296795.7:c.*921T>A | ENSP00000296795.2:n.*921T>A | |
| NM_003265.3:c.*921T>A MANE Select | NP_003256.1:n.*921T>A |