Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81642817T>C , CM000665.2:g.81642817T>C | GRCh38 |
| NC_000003.11:g.81691968T>C , CM000665.1:g.81691968T>C | GRCh37 |
| NC_000003.10:g.81774658T>C | NCBI36 |
| NG_011810.1:g.123984A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000158.4:c.956A>G MANE Select | NP_000149.4:p.His319Arg |
| ENST00000429644.7:c.956A>G MANE Select | ENSP00000410833.2:p.His319Arg |
| NM_000158.3:c.956A>G | NP_000149.3:p.His319Arg |
| ENST00000429644.6:c.956A>G | ENSP00000410833.2:p.His319Arg |
| ENST00000489715.1:c.833A>G | ENSP00000419638.1:p.His278Arg |
| ENST00000498468.1:n.506A>G |