Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119922646C>T , CM000663.2:g.119922646C>T | GRCh38 |
| NC_000001.10:g.120465269C>T , CM000663.1:g.120465269C>T | GRCh37 |
| NC_000001.9:g.120266792C>T | NCBI36 |
| NG_008163.1:g.152008G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_024408.4:c.4992G>A MANE Select | NP_077719.2:p.Val1664= |
| ENST00000256646.7:c.4992G>A MANE Select | ENSP00000256646.2:p.Val1664= |
| NM_024408.3:c.4992G>A | NP_077719.2:p.Val1664= |
| ENST00000256646.6:c.4992G>A | ENSP00000256646.2:p.Val1664= |
| ENST00000493703.1:n.402G>A | |
| XM_005270901.2:c.4875G>A | XP_005270958.1:p.Val1625= |
| XM_011541519.1:c.4980G>A | XP_011539821.1:p.Val1660= |
| XM_011541520.1:c.4875G>A | XP_011539822.1:p.Val1625= |