HGVS | Genome Assembly |
---|---|
NC_000001.11:g.161589929C>T , CM000663.2:g.161589929C>T | GRCh38 |
NC_000001.10:g.161559719C>T , CM000663.1:g.161559719C>T | GRCh37 |
NC_000001.9:g.159826343C>T | NCBI36 |
NG_011982.1:g.13591C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699402.1:c.41-40898G>A | ENSP00000514363.1:n.41-40898G>A | |
ENST00000699403.1:c.61+40439G>A | ENSP00000514364.1:n.61+40439G>A | |
ENST00000465075.6:n.483+110C>T | ||
ENST00000466542.6:c.391+110C>T | ENSP00000426627.1:n.391+110C>T | |
ENST00000473530.6:n.572+110C>T | ||
ENST00000473712.6:n.413+110C>T | ||
ENST00000482226.2:n.370+110C>T | ||
ENST00000543859.5:c.388+110C>T | ENSP00000444663.2:n.388+110C>T | |
ENST00000611236.1:c.388+110C>T | ENSP00000480953.1:n.388+110C>T | |
NR_047648.1:n.490+110C>T |