Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99420649C= , CM000666.2:g.99420649C= | GRCh38 |
| NC_000004.11:g.100341806C= , CM000666.1:g.100341806C= | GRCh37 |
| NC_000004.10:g.100560829C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000437033.7:c.709G= MANE Select | ENSP00000414254.2:p.Ala237= | |
| ENST00000209665.8:c.745G= | ENSP00000209665.4:p.Ala249= | |
| ENST00000437033.6:c.709G= | ENSP00000414254.2:p.Ala237= | |
| ENST00000476959.5:c.769G= | ENSP00000420269.1:p.Ala257= | |
| ENST00000482593.5:c.538G= | ENSP00000420613.1:p.Ala180= | |
| NM_000673.4:c.745G= | NP_000664.2:p.Ala249= | |
| NM_001166504.1:c.769G= | NP_001159976.1:p.Ala257= | |
| NM_000673.7:c.709G= MANE Select | NP_000664.3:p.Ala237= | |
| NM_001166504.2:c.769G= | NP_001159976.1:p.Ala257= |