Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.47325455G>A , CM000672.2:g.47325455G>A | GRCh38 |
| NC_000010.10:g.48413907C>T , CM000672.1:g.48413907C>T | GRCh37 |
| NC_000010.9:g.48033913C>T | NCBI36 |
| NG_033916.1:g.7966G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_016204.4:c.961G>A MANE Select | NP_057288.1:p.Ala321Thr |
| ENST00000581492.3:c.961G>A MANE Select | ENSP00000463051.1:p.Ala321Thr |
| NM_016204.2:c.961G>A | NP_057288.1:p.Ala321Thr |
| NM_016204.3:c.961G>A | NP_057288.1:p.Ala321Thr |
| ENST00000581492.2:c.961G>A | ENSP00000463051.1:p.Ala321Thr |
| XM_006717761.2:c.961G>A | XP_006717824.1:p.Ala321Thr |