Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94029601C>A , CM000663.2:g.94029601C>A | GRCh38 |
| NC_000001.10:g.94495157C>A , CM000663.1:g.94495157C>A | GRCh37 |
| NC_000001.9:g.94267745C>A | NCBI36 |
| NG_009073.1:g.96549G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.4383G>T MANE Select | NP_000341.2:p.Trp1461Cys |
| ENST00000370225.4:c.4383G>T MANE Select | ENSP00000359245.3:p.Trp1461Cys |
| NM_000350.2:c.4383G>T | NP_000341.2:p.Trp1461Cys |
| ENST00000370225.3:c.4383G>T | ENSP00000359245.3:p.Trp1461Cys |
| ENST00000536513.5:c.759G>T | ENSP00000439707.2:p.Trp253Cys |