Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.43169153C= , CM000683.2:g.43169153C= | GRCh38 |
| NG_009823.1:g.5123C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291554.6:c.54C= MANE Select | ENSP00000291554.2:p.Tyr18= | |
| ENST00000482775.1:n.67C= | ||
| NM_000394.3:c.54C= | NP_000385.1:p.Tyr18= | |
| XR_001755073.1:n.647+1884G= | ||
| NM_000394.4:c.54C= MANE Select | NP_000385.1:p.Tyr18= |