Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.16125304C= , CM000663.2:g.16125304C= | GRCh38 |
| NC_000001.10:g.16451799C= , CM000663.1:g.16451799C= | GRCh37 |
| NC_000001.9:g.16324386C= | NCBI36 |
| NG_021396.1:g.35784G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358432.8:c.2842G= MANE Select | ENSP00000351209.5:p.Gly948= | |
| ENST00000358432.7:c.2842G= | ENSP00000351209.5:p.Gly948= | |
| NM_004431.3:c.2842G= | NP_004422.2:p.Gly948= | |
| NM_001329090.1:c.2680G= | NP_001316019.1:p.Gly894= | |
| NM_004431.4:c.2842G= | NP_004422.2:p.Gly948= | |
| NM_004431.5:c.2842G= MANE Select | NP_004422.2:p.Gly948= | |
| NM_001329090.2:c.2680G= | NP_001316019.1:p.Gly894= |