Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.99221719C>T , CM000671.2:g.99221719C>T | GRCh38 |
| NC_000009.11:g.101984001C>T , CM000671.1:g.101984001C>T | GRCh37 |
| NC_000009.10:g.101023822C>T | NCBI36 |
| NG_008928.1:g.5246G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_033087.4:c.176G>A MANE Select | NP_149078.1:p.Cys59Tyr |
| ENST00000476832.2:c.176G>A MANE Select | ENSP00000417764.1:p.Cys59Tyr |
| NM_033087.3:c.176G>A | NP_149078.1:p.Cys59Tyr |
| NR_024532.1:n.246G>A | |
| NR_024532.2:n.224G>A | |
| ENST00000238477.5:c.176G>A | ENSP00000432675.2:p.Cys59Tyr |
| ENST00000476832.1:c.176G>A | ENSP00000417764.1:p.Cys59Tyr |