HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94942325G= , CM000672.2:g.94942325G= | GRCh38 |
NC_000010.10:g.96702082G= , CM000672.1:g.96702082G= | GRCh37 |
NC_000010.9:g.96692072G= | NCBI36 |
NG_008385.1:g.8668G= | |
NG_008385.2:g.9168G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.465G= MANE Select | ENSP00000260682.6:p.Glu155= | |
ENST00000643112.1:c.465G= | ENSP00000496202.1:p.Glu155= | |
ENST00000645207.1:n.618G= | ||
ENST00000260682.6:c.465G= | ENSP00000260682.6:p.Glu155= | |
ENST00000461906.1:n.490G= | ||
ENST00000473496.1:n.236G= | ||
NM_000771.3:c.465G= | NP_000762.2:p.Glu155= | |
NM_000771.4:c.465G= MANE Select | NP_000762.2:p.Glu155= |