HGVS | Genome Assembly |
---|---|
NC_000017.11:g.58273562G>T , CM000679.2:g.58273562G>T | GRCh38 |
NC_000017.10:g.56350923G>T , CM000679.1:g.56350923G>T | GRCh37 |
NC_000017.9:g.53705922G>T | NCBI36 |
NG_009629.1:g.12374C>A , LRG_84:g.12374C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000578493.2:n.806C>A | ||
ENST00000699291.1:c.598C>A | ENSP00000514272.1:n.598C>A | |
ENST00000699292.1:n.513C>A | ||
ENST00000225275.4:c.1473C>A MANE Select | ENSP00000225275.3:p.Ala491= | |
ENST00000225275.3:c.1473C>A | ENSP00000225275.3:p.Ala491= | |
NM_000250.1:c.1473C>A , LRG_84t1:c.1473C>A | NP_000241.1:p.Ala491= | |
XM_011524821.1:c.1659C>A | XP_011523123.1:p.Ala553= | |
XM_011524822.1:c.1188C>A | XP_011523124.1:p.Ala396= | |
XM_011524823.1:c.*22C>A | XP_011523125.1:n.*22C>A | |
NM_000250.2:c.1473C>A MANE Select | NP_000241.1:p.Ala491= |