HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44292394A>T , CM000683.2:g.44292394A>T | GRCh38 |
NC_000021.8:g.45712277A>T , CM000683.1:g.45712277A>T | GRCh37 |
NC_000021.7:g.44536705A>T | NCBI36 |
NG_009556.1:g.11515A>T , LRG_18:g.11515A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000291582.6:c.1088A>T MANE Select | ENSP00000291582.5:p.Glu363Val | |
ENST00000291582.5:c.1088A>T | ENSP00000291582.5:p.Glu363Val | |
ENST00000337909.5:n.549A>T | ||
ENST00000397994.8:n.549A>T | ||
ENST00000527919.5:n.1818A>T | ||
ENST00000530812.5:n.2835A>T | ||
NM_000383.3:c.1088A>T | NP_000374.1:p.Glu363Val | |
XM_011529551.1:c.1085A>T | XP_011527853.1:p.Glu362Val | |
NM_000383.4:c.1088A>T MANE Select | NP_000374.1:p.Glu363Val |