HGVS | Genome Assembly |
---|---|
NC_000001.11:g.110174012G>A , CM000663.2:g.110174012G>A | GRCh38 |
NC_000001.10:g.110716634G>A , CM000663.1:g.110716634G>A | GRCh37 |
NC_000001.9:g.110518157G>A | NCBI36 |
NG_051945.1:g.28499G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331565.5:c.484G>A MANE Select | ENSP00000330199.3:p.Gly162Arg | |
ENST00000331565.4:c.484G>A | ENSP00000330199.3:p.Gly162Arg | |
NM_001010898.2:c.484G>A | NP_001010898.1:p.Gly162Arg | |
XM_006710643.1:c.484G>A | XP_006710706.1:p.Gly162Arg | |
NM_001010898.3:c.484G>A | NP_001010898.1:p.Gly162Arg | |
XM_006710643.2:c.484G>A | XP_006710706.1:p.Gly162Arg | |
NM_001010898.4:c.484G>A MANE Select | NP_001010898.1:p.Gly162Arg |