HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169525949C= , CM000663.2:g.169525949C= | GRCh38 |
NC_000001.10:g.169495187C= , CM000663.1:g.169495187C= | GRCh37 |
NC_000001.9:g.167761811C= | NCBI36 |
NG_011806.1:g.65583G= , LRG_553:g.65583G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367797.9:c.5668G= MANE Select | ENSP00000356771.3:p.Glu1890= | |
ENST00000367796.3:c.5683G= | ENSP00000356770.3:p.Glu1895= | |
ENST00000367797.7:c.5668G= | ENSP00000356771.3:p.Glu1890= | |
NM_000130.4:c.5668G= , LRG_553t1:c.5668G= | NP_000121.2:p.Glu1890= | |
XM_017000660.2:c.5257G= | XP_016856149.1:p.Glu1753= | |
NM_000130.5:c.5668G= MANE Select | NP_000121.2:p.Glu1890= |