Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.144399847C= , CM000669.2:g.144399847C= | GRCh38 |
| NC_000007.13:g.144096940C= , CM000669.1:g.144096940C= | GRCh37 |
| NC_000007.12:g.143727873C= | NCBI36 |
| NG_028979.1:g.15381G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001080413.3:c.1064G= MANE Select | NP_001073882.3:p.Arg355= |
| ENST00000467773.1:c.1064G= MANE Select | ENSP00000419457.1:p.Arg355= |
| ENST00000483238.5:c.968G= | ENSP00000419565.1:p.Arg323= |
| ENST00000643164.1:c.161G= | ENSP00000495343.1:p.Arg54= |
| ENST00000645489.1:c.713G= | ENSP00000496732.1:p.Arg238= |
| XM_011515791.1:c.713G= | XP_011514093.1:p.Arg238= |
| XM_017011742.2:c.968G= | XP_016867231.1:p.Arg323= |