Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.84840312T>A , CM000677.2:g.84840312T>A | GRCh38 |
| NC_000015.9:g.85383543T>A , CM000677.1:g.85383543T>A | GRCh37 |
| NC_000015.8:g.83184547T>A | NCBI36 |
| NG_054748.1:g.28682T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258888.6:c.1033T>A MANE Select | ENSP00000258888.6:p.Cys345Ser | |
| ENST00000258888.5:c.1639T>A | ENSP00000258888.5:p.Cys547Ser | |
| NM_020778.4:c.1639T>A | NP_065829.3:p.Cys547Ser | |
| NM_020778.5:c.1033T>A MANE Select | NP_065829.4:p.Cys345Ser |