Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.47325313G>A , CM000672.2:g.47325313G>A | GRCh38 |
| NC_000010.10:g.48414049C>T , CM000672.1:g.48414049C>T | GRCh37 |
| NC_000010.9:g.48034055C>T | NCBI36 |
| NG_033916.1:g.7824G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000581492.3:c.819G>A MANE Select | ENSP00000463051.1:p.Arg273= | |
| ENST00000581492.2:c.819G>A | ENSP00000463051.1:p.Arg273= | |
| NM_016204.2:c.819G>A | NP_057288.1:p.Arg273= | |
| XM_006717761.2:c.819G>A | XP_006717824.1:p.Arg273= | |
| NM_016204.3:c.819G>A | NP_057288.1:p.Arg273= | |
| NM_016204.4:c.819G>A MANE Select | NP_057288.1:p.Arg273= |