Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81490442C>T , CM000665.2:g.81490442C>T | GRCh38 |
| NC_000003.11:g.81539593C>T , CM000665.1:g.81539593C>T | GRCh37 |
| NC_000003.10:g.81622283C>T | NCBI36 |
| NG_011810.1:g.276359G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000158.4:c.2074G>A MANE Select | NP_000149.4:p.Ala692Thr |
| ENST00000429644.7:c.2074G>A MANE Select | ENSP00000410833.2:p.Ala692Thr |
| NM_000158.3:c.2074G>A | NP_000149.3:p.Ala692Thr |
| ENST00000429644.6:c.2074G>A | ENSP00000410833.2:p.Ala692Thr |
| ENST00000489715.1:c.1951G>A | ENSP00000419638.1:p.Ala651Thr |