Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180659561G= , CM000665.2:g.180659561G= | GRCh38 |
| NC_000003.11:g.180377349G= , CM000665.1:g.180377349G= | GRCh37 |
| NC_000003.10:g.181860043G= | NCBI36 |
| NG_029581.1:g.24935C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476379.6:c.629C= MANE Select | ENSP00000417960.2:p.Ala210= | |
| ENST00000650641.1:n.708C= | ||
| ENST00000650889.1:n.801C= | ||
| ENST00000651046.1:c.629C= | ENSP00000499175.1:p.Ala210= | |
| ENST00000651818.1:n.771C= | ||
| ENST00000652024.1:n.720C= | ||
| ENST00000652408.1:n.766C= | ||
| ENST00000442201.6:c.629C= | ENSP00000405708.2:p.Ala210= | |
| ENST00000476379.5:c.629C= | ENSP00000417960.1:p.Ala210= | |
| NM_181426.1:c.629C= | NP_852091.1:p.Ala210= | |
| NM_181426.2:c.629C= MANE Select | NP_852091.1:p.Ala210= |