HGVS | Genome Assembly |
---|---|
NC_000001.11:g.161589870A>T , CM000663.2:g.161589870A>T | GRCh38 |
NC_000001.10:g.161559660A>T , CM000663.1:g.161559660A>T | GRCh37 |
NC_000001.9:g.159826284A>T | NCBI36 |
NG_011982.1:g.13532A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699402.1:c.41-40839T>A | ENSP00000514363.1:n.41-40839T>A | |
ENST00000699403.1:c.61+40498T>A | ENSP00000514364.1:n.61+40498T>A | |
ENST00000465075.6:n.483+51A>T | ||
ENST00000466542.6:c.391+51A>T | ENSP00000426627.1:n.391+51A>T | |
ENST00000473530.6:n.572+51A>T | ||
ENST00000473712.6:n.413+51A>T | ||
ENST00000482226.2:n.370+51A>T | ||
ENST00000496692.6:n.538A>T | ||
ENST00000543859.5:c.388+51A>T | ENSP00000444663.2:n.388+51A>T | |
ENST00000611236.1:c.388+51A>T | ENSP00000480953.1:n.388+51A>T | |
NR_047648.1:n.490+51A>T |