HGVS | Genome Assembly |
---|---|
NC_000001.11:g.161589900A= , CM000663.2:g.161589900A= | GRCh38 |
NC_000001.10:g.161559690A= , CM000663.1:g.161559690A= | GRCh37 |
NC_000001.9:g.159826314A= | NCBI36 |
NG_011982.1:g.13562A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699402.1:c.41-40869T= | ENSP00000514363.1:n.41-40869T= | |
ENST00000699403.1:c.61+40468T= | ENSP00000514364.1:n.61+40468T= | |
ENST00000465075.6:n.483+81A= | ||
ENST00000466542.6:c.391+81A= | ENSP00000426627.1:n.391+81A= | |
ENST00000473530.6:n.572+81A= | ||
ENST00000473712.6:n.413+81A= | ||
ENST00000482226.2:n.370+81A= | ||
ENST00000543859.5:c.388+81A= | ENSP00000444663.2:n.388+81A= | |
ENST00000611236.1:c.388+81A= | ENSP00000480953.1:n.388+81A= | |
NR_047648.1:n.490+81A= |