Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122462018C>A , CM000672.2:g.122462018C>A | GRCh38 |
| NC_000010.10:g.124221534C>A , CM000672.1:g.124221534C>A | GRCh37 |
| NC_000010.9:g.124211524C>A | NCBI36 |
| NG_011554.1:g.5494C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.366C>A MANE Select | ENSP00000357980.3:p.Asp122Glu | |
| ENST00000648167.1:c.154+3309C>A | ENSP00000498033.1:n.154+3309C>A | |
| ENST00000368984.7:c.366C>A | ENSP00000357980.3:p.Asp122Glu | |
| NM_002775.4:c.366C>A | NP_002766.1:p.Asp122Glu | |
| NM_002775.5:c.366C>A MANE Select | NP_002766.1:p.Asp122Glu |