HGVS | Genome Assembly |
---|---|
NC_000017.11:g.58273570G= , CM000679.2:g.58273570G= | GRCh38 |
NC_000017.10:g.56350931G= , CM000679.1:g.56350931G= | GRCh37 |
NC_000017.9:g.53705930G= | NCBI36 |
NG_009629.1:g.12366C= , LRG_84:g.12366C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000578493.2:n.798C= | ||
ENST00000699291.1:c.590C= | ENSP00000514272.1:n.590C= | |
ENST00000699292.1:n.505C= | ||
ENST00000225275.4:c.1465C= MANE Select | ENSP00000225275.3:p.Arg489= | |
ENST00000225275.3:c.1465C= | ENSP00000225275.3:p.Arg489= | |
NM_000250.1:c.1465C= , LRG_84t1:c.1465C= | NP_000241.1:p.Arg489= | |
XM_011524821.1:c.1651C= | XP_011523123.1:p.Arg551= | |
XM_011524822.1:c.1180C= | XP_011523124.1:p.Arg394= | |
XM_011524823.1:c.*14C= | XP_011523125.1:n.*14C= | |
NM_000250.2:c.1465C= MANE Select | NP_000241.1:p.Arg489= |