HGVS | Genome Assembly |
---|---|
NC_000005.10:g.146339764C>A , CM000667.2:g.146339764C>A | GRCh38 |
NC_000005.9:g.145719327C>A , CM000667.1:g.145719327C>A | GRCh37 |
NC_000005.8:g.145699520C>A | NCBI36 |
NG_011885.1:g.5741C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000646991.2:c.337C>A MANE Select | ENSP00000495718.1:p.Gln113Lys | |
ENST00000230732.4:c.337C>A | ENSP00000230732.4:p.Gln113Lys | |
NM_002700.2:c.337C>A | NP_002691.1:p.Gln113Lys | |
NM_002700.3:c.337C>A MANE Select | NP_002691.1:p.Gln113Lys |