Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122506874G>A , CM000672.2:g.122506874G>A | GRCh38 |
| NC_000010.10:g.124266390G>A , CM000672.1:g.124266390G>A | GRCh37 |
| NC_000010.9:g.124256380G>A | NCBI36 |
| NG_011554.1:g.50350G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002775.5:c.961G>A MANE Select | NP_002766.1:p.Ala321Thr |
| ENST00000368984.8:c.961G>A MANE Select | ENSP00000357980.3:p.Ala321Thr |
| NM_002775.4:c.961G>A | NP_002766.1:p.Ala321Thr |
| ENST00000368984.7:c.961G>A | ENSP00000357980.3:p.Ala321Thr |
| ENST00000420892.1:c.184G>A | ENSP00000412676.1:p.Ala62Thr |
| ENST00000648167.1:c.643G>A | ENSP00000498033.1:p.Ala215Thr |