HGVS | Genome Assembly |
---|---|
NC_000017.11:g.49991722G>T , CM000679.2:g.49991722G>T | GRCh38 |
NC_000017.10:g.48069086G>T , CM000679.1:g.48069086G>T | GRCh37 |
NC_000017.9:g.45424085G>T | NCBI36 |
NG_023063.1:g.8503C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000434704.2:c.659C>A MANE Select | ENSP00000389870.2:p.Ser220Tyr | |
ENST00000512495.2:c.299C>A | ENSP00000449976.1:p.Ser100Tyr | |
NM_005220.2:c.659C>A | NP_005211.1:p.Ser220Tyr | |
XM_011524458.1:c.516+1678C>A | XP_011522760.1:n.516+1678C>A | |
NM_005220.3:c.659C>A MANE Select | NP_005211.1:p.Ser220Tyr |