Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180660593G>A , CM000665.2:g.180660593G>A | GRCh38 |
| NC_000003.11:g.180378381G>A , CM000665.1:g.180378381G>A | GRCh37 |
| NC_000003.10:g.181861075G>A | NCBI36 |
| NG_029581.1:g.23903C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_181426.2:c.493C>T MANE Select | NP_852091.1:p.Gln165Ter |
| ENST00000476379.6:c.493C>T MANE Select | ENSP00000417960.2:p.Gln165Ter |
| NM_181426.1:c.493C>T | NP_852091.1:p.Gln165Ter |
| ENST00000442201.6:c.493C>T | ENSP00000405708.2:p.Gln165Ter |
| ENST00000476379.5:c.493C>T | ENSP00000417960.1:p.Gln165Ter |
| ENST00000650641.1:n.572C>T | |
| ENST00000650889.1:n.665C>T | |
| ENST00000651046.1:c.493C>T | ENSP00000499175.1:p.Gln165Ter |
| ENST00000651818.1:n.635C>T | |
| ENST00000652024.1:n.584C>T | |
| ENST00000652408.1:n.630C>T |