HGVS | Genome Assembly |
---|---|
NC_000020.11:g.44115726G= , CM000682.2:g.44115726G= | GRCh38 |
NC_000020.10:g.42744366G= , CM000682.1:g.42744366G= | GRCh37 |
NC_000020.9:g.42177780G= | NCBI36 |
NG_031867.1:g.76853C= , LRG_394:g.76853C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372980.4:c.1949C= MANE Select | ENSP00000362071.3:p.Ala650= | |
ENST00000372980.3:c.1949C= | ENSP00000362071.3:p.Ala650= | |
NM_020433.4:c.1949C= , LRG_394t1:c.1949C= | NP_065166.2:p.Ala650= | |
XM_006723832.2:c.1949C= | XP_006723895.1:p.Ala650= | |
NM_020433.5:c.1949C= MANE Select | NP_065166.2:p.Ala650= |