Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180644141A= , CM000665.2:g.180644141A= | GRCh38 |
| NC_000003.11:g.180361929A= , CM000665.1:g.180361929A= | GRCh37 |
| NC_000003.10:g.181844623A= | NCBI36 |
| NG_029581.1:g.40355T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_181426.2:c.1644T= MANE Select | NP_852091.1:p.Asp548= |
| ENST00000476379.6:c.1644T= MANE Select | ENSP00000417960.2:p.Asp548= |
| NM_181426.1:c.1644T= | NP_852091.1:p.Asp548= |
| ENST00000442201.6:c.1644T= | ENSP00000405708.2:p.Asp548= |
| ENST00000476379.5:c.1644T= | ENSP00000417960.1:p.Asp548= |
| ENST00000650641.1:n.1531T= | |
| ENST00000650889.1:n.4856T= | |
| ENST00000651046.1:c.1452T= | ENSP00000499175.1:p.Asp484= |
| ENST00000651818.1:n.1594T= | |
| ENST00000651922.1:n.969T= | |
| ENST00000652024.1:n.4364T= | |
| ENST00000652408.1:n.1781T= |