HGVS | Genome Assembly |
---|---|
NC_000020.11:g.57562834A>G , CM000682.2:g.57562834A>G | GRCh38 |
NC_000020.10:g.56137890A>G , CM000682.1:g.56137890A>G | GRCh37 |
NC_000020.9:g.55571296A>G | NCBI36 |
NG_008205.1:g.6754A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000319441.6:c.545A>G MANE Select | ENSP00000319814.4:p.Glu182Gly | |
ENST00000319441.5:c.545A>G | ENSP00000319814.4:p.Glu182Gly | |
ENST00000467047.1:n.1755A>G | ||
ENST00000470051.1:n.1A>G | ||
ENST00000498194.1:n.487A>G | ||
NM_002591.3:c.545A>G | NP_002582.3:p.Glu182Gly | |
XM_011528839.1:c.149A>G | XP_011527141.1:p.Glu50Gly | |
XM_024451888.1:c.149A>G | XP_024307656.1:p.Glu50Gly | |
NM_002591.4:c.545A>G MANE Select | NP_002582.3:p.Glu182Gly |