Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7581494G>A , CM000679.2:g.7581494G>A | GRCh38 |
| NC_000017.10:g.7484812G>A , CM000679.1:g.7484812G>A | GRCh37 |
| NC_000017.9:g.7425536G>A | NCBI36 |
| NG_009204.1:g.2848G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001251.3:c.1048G>A MANE Select | NP_001242.2:p.Ala350Thr |
| ENST00000250092.11:c.1048G>A MANE Select | ENSP00000250092.6:p.Ala350Thr |
| NM_001040059.1:c.967G>A | NP_001035148.1:p.Ala323Thr |
| NM_001040059.2:c.967G>A | NP_001035148.1:p.Ala323Thr |
| NM_001251.2:c.1048G>A | NP_001242.2:p.Ala350Thr |
| ENST00000250092.10:c.1048G>A | ENSP00000250092.6:p.Ala350Thr |
| ENST00000380498.10:c.967G>A | ENSP00000369867.6:p.Ala323Thr |
| ENST00000584180.1:c.763G>A |