Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81642983C>G , CM000665.2:g.81642983C>G | GRCh38 |
| NC_000003.11:g.81692134C>G , CM000665.1:g.81692134C>G | GRCh37 |
| NC_000003.10:g.81774824C>G | NCBI36 |
| NG_011810.1:g.123818G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000158.4:c.790G>C MANE Select | NP_000149.4:p.Gly264Arg |
| ENST00000429644.7:c.790G>C MANE Select | ENSP00000410833.2:p.Gly264Arg |
| NM_000158.3:c.790G>C | NP_000149.3:p.Gly264Arg |
| ENST00000429644.6:c.790G>C | ENSP00000410833.2:p.Gly264Arg |
| ENST00000489715.1:c.667G>C | ENSP00000419638.1:p.Gly223Arg |
| ENST00000498468.1:n.340G>C |