HGVS | Genome Assembly |
---|---|
NC_000003.12:g.180659496C= , CM000665.2:g.180659496C= | GRCh38 |
NC_000003.11:g.180377284C= , CM000665.1:g.180377284C= | GRCh37 |
NC_000003.10:g.181859978C= | NCBI36 |
NG_029581.1:g.25000G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000476379.6:c.694G= MANE Select | ENSP00000417960.2:p.Glu232= | |
ENST00000650641.1:n.773G= | ||
ENST00000650889.1:n.866G= | ||
ENST00000651046.1:c.694G= | ENSP00000499175.1:p.Glu232= | |
ENST00000651818.1:n.836G= | ||
ENST00000652024.1:n.785G= | ||
ENST00000652408.1:n.831G= | ||
ENST00000442201.6:c.694G= | ENSP00000405708.2:p.Glu232= | |
ENST00000476379.5:c.694G= | ENSP00000417960.1:p.Glu232= | |
NM_181426.1:c.694G= | NP_852091.1:p.Glu232= | |
NM_181426.2:c.694G= MANE Select | NP_852091.1:p.Glu232= |