Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122489603G= , CM000672.2:g.122489603G= | GRCh38 |
| NC_000010.10:g.124249119G= , CM000672.1:g.124249119G= | GRCh37 |
| NC_000010.9:g.124239109G= | NCBI36 |
| NG_011554.1:g.33079G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002775.5:c.754G= MANE Select | NP_002766.1:p.Ala252= |
| ENST00000368984.8:c.754G= MANE Select | ENSP00000357980.3:p.Ala252= |
| NM_002775.4:c.754G= | NP_002766.1:p.Ala252= |
| ENST00000368984.7:c.754G= | ENSP00000357980.3:p.Ala252= |
| ENST00000648167.1:c.436G= | ENSP00000498033.1:p.Ala146= |