HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571287G>A , CM000663.2:g.154571287G>A | GRCh38 |
NC_000001.10:g.154543763G>A , CM000663.1:g.154543763G>A | GRCh37 |
NC_000001.9:g.152810387G>A | NCBI36 |
NG_008027.1:g.8507G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.464G>A MANE Select | ENSP00000357461.3:p.Cys155Tyr | |
ENST00000636034.1:c.464G>A | ENSP00000489703.1:p.Cys155Tyr | |
ENST00000637900.1:c.470G>A | ENSP00000490474.1:p.Cys157Tyr | |
ENST00000368476.3:c.464G>A | ENSP00000357461.3:p.Cys155Tyr | |
NM_000748.2:c.464G>A | NP_000739.1:p.Cys155Tyr | |
XM_017000180.2:c.-9-38G>A | XP_016855669.1:n.-9-38G>A | |
XR_001736952.2:n.716G>A | ||
NM_000748.3:c.464G>A MANE Select | NP_000739.1:p.Cys155Tyr |