Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180619952C>A , CM000665.2:g.180619952C>A | GRCh38 |
| NC_000003.11:g.180337740C>A , CM000665.1:g.180337740C>A | GRCh37 |
| NC_000003.10:g.181820434C>A | NCBI36 |
| NG_029581.1:g.64544G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_181426.2:c.2017G>T MANE Select | NP_852091.1:p.Glu673Ter |
| ENST00000476379.6:c.2017G>T MANE Select | ENSP00000417960.2:p.Glu673Ter |
| NM_181426.1:c.2017G>T | NP_852091.1:p.Glu673Ter |
| ENST00000442201.6:c.2017G>T | ENSP00000405708.2:p.Glu673Ter |
| ENST00000476379.5:c.1999-587G>T | ENSP00000417960.1:n.1999-587G>T |
| ENST00000650641.1:n.1904G>T | |
| ENST00000651046.1:c.1825G>T | ENSP00000499175.1:p.Glu609Ter |
| ENST00000651922.1:n.1342G>T | |
| ENST00000652010.1:n.1648G>T | |
| ENST00000652408.1:n.2154G>T |