HGVS | Genome Assembly |
---|---|
NC_000002.12:g.31531451C= , CM000664.2:g.31531451C= | GRCh38 |
NC_000002.11:g.31756521C= , CM000664.1:g.31756521C= | GRCh37 |
NC_000002.10:g.31610025C= | NCBI36 |
NG_008365.1:g.54521G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000622030.2:c.467G= MANE Select | ENSP00000477587.1:p.Gly156= | |
ENST00000622030.1:c.467G= | ENSP00000477587.1:p.Gly156= | |
NM_000348.3:c.467G= | NP_000339.2:p.Gly156= | |
XM_011533069.1:c.245G= | XP_011531371.1:p.Gly82= | |
XM_011533070.1:c.212G= | XP_011531372.1:p.Gly71= | |
XM_011533071.1:c.212G= | XP_011531373.1:p.Gly71= | |
XM_011533072.1:c.212G= | XP_011531374.1:p.Gly71= | |
XM_011533069.2:c.245G= | XP_011531371.1:p.Gly82= | |
XM_011533072.2:c.212G= | XP_011531374.1:p.Gly71= | |
NM_000348.4:c.467G= MANE Select | NP_000339.2:p.Gly156= |