Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122461941G>T , CM000672.2:g.122461941G>T | GRCh38 |
| NC_000010.10:g.124221457G>T , CM000672.1:g.124221457G>T | GRCh37 |
| NC_000010.9:g.124211447G>T | NCBI36 |
| NG_011554.1:g.5417G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.289G>T MANE Select | ENSP00000357980.3:p.Ala97Ser | |
| ENST00000648167.1:c.154+3232G>T | ENSP00000498033.1:n.154+3232G>T | |
| ENST00000368984.7:c.289G>T | ENSP00000357980.3:p.Ala97Ser | |
| NM_002775.4:c.289G>T | NP_002766.1:p.Ala97Ser | |
| NM_002775.5:c.289G>T MANE Select | NP_002766.1:p.Ala97Ser |