Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.83368038C>T , CM000669.2:g.83368038C>T | GRCh38 |
| NC_000007.13:g.82997354C>T , CM000669.1:g.82997354C>T | GRCh37 |
| NC_000007.12:g.82835290C>T | NCBI36 |
| NG_021242.1:g.286126G>A | |
| NG_021242.2:g.286126G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000427262.6:c.1696G>A | ENSP00000405052.1:p.Val566Met | |
| ENST00000643230.2:c.1876G>A MANE Select | ENSP00000496491.1:p.Val626Met | |
| ENST00000643441.1:n.1861G>A | ||
| ENST00000307792.7:c.1876G>A | ENSP00000303212.3:p.Val626Met | |
| ENST00000427262.5:c.1696G>A | ENSP00000405052.1:p.Val566Met | |
| NM_001178129.1:c.1696G>A | NP_001171600.1:p.Val566Met | |
| NM_012431.2:c.1876G>A | NP_036563.1:p.Val626Met | |
| NM_012431.3:c.1876G>A MANE Select | NP_036563.1:p.Val626Met | |
| NM_001178129.2:c.1696G>A | NP_001171600.1:p.Val566Met |