Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56043402G>A , CM000674.2:g.56043402G>A | GRCh38 |
| NC_000012.11:g.56437186G>A , CM000674.1:g.56437186G>A | GRCh37 |
| NC_000012.10:g.54723453G>A | NCBI36 |
| NG_023201.1:g.6501G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001029.5:c.221G>A MANE Select | NP_001020.2:p.Cys74Tyr |
| ENST00000646449.2:c.221G>A MANE Select | ENSP00000496643.1:p.Cys74Tyr |
| NM_001029.3:c.221G>A | NP_001020.2:p.Cys74Tyr |
| ENST00000356464.10:c.221G>A | ENSP00000348849.5:p.Cys74Tyr |
| ENST00000356464.9:c.221G>A | ENSP00000348849.5:p.Cys74Tyr |
| ENST00000548590.1:n.1008G>A | |
| ENST00000552361.1:c.221G>A | ENSP00000450339.1:p.Cys74Tyr |