Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180641993C= , CM000665.2:g.180641993C= | GRCh38 |
| NC_000003.11:g.180359781C= , CM000665.1:g.180359781C= | GRCh37 |
| NC_000003.10:g.181842475C= | NCBI36 |
| NG_029581.1:g.42503G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_181426.2:c.1874G= MANE Select | NP_852091.1:p.Ser625= |
| ENST00000476379.6:c.1874G= MANE Select | ENSP00000417960.2:p.Ser625= |
| NM_181426.1:c.1874G= | NP_852091.1:p.Ser625= |
| ENST00000442201.6:c.1874G= | ENSP00000405708.2:p.Ser625= |
| ENST00000476379.5:c.1874G= | ENSP00000417960.1:p.Ser625= |
| ENST00000650641.1:n.1761G= | |
| ENST00000651046.1:c.1682G= | ENSP00000499175.1:p.Ser561= |
| ENST00000651922.1:n.1199G= | |
| ENST00000652408.1:n.2011G= |