Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.16148725C= , CM000663.2:g.16148725C= | GRCh38 |
| NC_000001.10:g.16475220C= , CM000663.1:g.16475220C= | GRCh37 |
| NC_000001.9:g.16347807C= | NCBI36 |
| NG_021396.1:g.12363G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358432.8:c.476G= MANE Select | ENSP00000351209.5:p.Arg159= | |
| ENST00000358432.7:c.476G= | ENSP00000351209.5:p.Arg159= | |
| ENST00000461614.1:n.528G= | ||
| NM_004431.3:c.476G= | NP_004422.2:p.Arg159= | |
| NM_001329090.1:c.314G= | NP_001316019.1:p.Arg105= | |
| NM_004431.4:c.476G= | NP_004422.2:p.Arg159= | |
| XM_017000537.1:c.476G= | XP_016856026.1:p.Arg159= | |
| NM_004431.5:c.476G= MANE Select | NP_004422.2:p.Arg159= | |
| NM_001329090.2:c.314G= | NP_001316019.1:p.Arg105= |