Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94005494G>A , CM000663.2:g.94005494G>A | GRCh38 |
| NC_000001.10:g.94471050G>A , CM000663.1:g.94471050G>A | GRCh37 |
| NC_000001.9:g.94243638G>A | NCBI36 |
| NG_009073.1:g.120656C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.6094C>T MANE Select | NP_000341.2:p.His2032Tyr |
| ENST00000370225.4:c.6094C>T MANE Select | ENSP00000359245.3:p.His2032Tyr |
| NM_000350.2:c.6094C>T | NP_000341.2:p.His2032Tyr |
| ENST00000370225.3:c.6094C>T | ENSP00000359245.3:p.His2032Tyr |
| ENST00000465352.1:n.510C>T | |
| ENST00000484388.1:n.208C>T | |
| ENST00000536513.5:c.2470C>T | ENSP00000439707.2:p.His824Tyr |