Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81642962C>A , CM000665.2:g.81642962C>A | GRCh38 |
| NC_000003.11:g.81692113C>A , CM000665.1:g.81692113C>A | GRCh37 |
| NC_000003.10:g.81774803C>A | NCBI36 |
| NG_011810.1:g.123839G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000158.4:c.811G>T MANE Select | NP_000149.4:p.Glu271Ter |
| ENST00000429644.7:c.811G>T MANE Select | ENSP00000410833.2:p.Glu271Ter |
| NM_000158.3:c.811G>T | NP_000149.3:p.Glu271Ter |
| ENST00000429644.6:c.811G>T | ENSP00000410833.2:p.Glu271Ter |
| ENST00000489715.1:c.688G>T | ENSP00000419638.1:p.Glu230Ter |
| ENST00000498468.1:n.361G>T |