Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94010821C= , CM000663.2:g.94010821C= | GRCh38 |
| NC_000001.10:g.94476377C= , CM000663.1:g.94476377C= | GRCh37 |
| NC_000001.9:g.94248965C= | NCBI36 |
| NG_009073.1:g.115329G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.5693G= MANE Select | NP_000341.2:p.Arg1898= |
| ENST00000370225.4:c.5693G= MANE Select | ENSP00000359245.3:p.Arg1898= |
| NM_000350.2:c.5693G= | NP_000341.2:p.Arg1898= |
| ENST00000370225.3:c.5693G= | ENSP00000359245.3:p.Arg1898= |
| ENST00000465352.1:n.109G= | |
| ENST00000536513.5:c.2069G= | ENSP00000439707.2:p.Arg690= |