HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52652078A>T , CM000674.2:g.52652078A>T | GRCh38 |
NC_000012.11:g.53045862A>T , CM000674.1:g.53045862A>T | GRCh37 |
NC_000012.10:g.51332129A>T | NCBI36 |
NG_008296.1:g.5098T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309680.4:c.65T>A MANE Select | ENSP00000310861.3:p.Phe22Tyr | |
ENST00000309680.3:c.65T>A | ENSP00000310861.3:p.Phe22Tyr | |
NM_000423.2:c.65T>A | NP_000414.2:p.Phe22Tyr | |
NM_000423.3:c.65T>A MANE Select | NP_000414.2:p.Phe22Tyr |