Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.191357118A>G , CM000665.2:g.191357118A>G | GRCh38 |
| NC_000003.11:g.191074907A>G , CM000665.1:g.191074907A>G | GRCh37 |
| NC_000003.10:g.192557601A>G | NCBI36 |
| NG_008994.1:g.33034A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392455.9:c.80A>G MANE Select | ENSP00000376249.4:p.His27Arg | |
| ENST00000392456.4:c.80A>G | ENSP00000376250.4:p.His27Arg | |
| ENST00000392455.7:c.80A>G | ENSP00000376249.3:p.His27Arg | |
| ENST00000392456.3:c.80A>G | ENSP00000376250.3:p.His27Arg | |
| NM_174908.3:c.80A>G | NP_777568.1:p.His27Arg | |
| NM_178335.2:c.80A>G | NP_848018.1:p.His27Arg | |
| XM_011512460.1:c.80A>G | XP_011510762.1:p.His27Arg | |
| NM_178335.3:c.80A>G MANE Select | NP_848018.1:p.His27Arg | |
| NM_174908.4:c.80A>G | NP_777568.1:p.His27Arg |