HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461918G>A , CM000672.2:g.122461918G>A | GRCh38 |
NC_000010.10:g.124221434G>A , CM000672.1:g.124221434G>A | GRCh37 |
NC_000010.9:g.124211424G>A | NCBI36 |
NG_011554.1:g.5394G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.266G>A MANE Select | ENSP00000357980.3:p.Cys89Tyr | |
ENST00000648167.1:c.154+3209G>A | ENSP00000498033.1:n.154+3209G>A | |
ENST00000368984.7:c.266G>A | ENSP00000357980.3:p.Cys89Tyr | |
NM_002775.4:c.266G>A | NP_002766.1:p.Cys89Tyr | |
NM_002775.5:c.266G>A MANE Select | NP_002766.1:p.Cys89Tyr |