HGVS | Genome Assembly |
---|---|
NC_000001.11:g.161589633C>T , CM000663.2:g.161589633C>T | GRCh38 |
NC_000001.10:g.161559423C>T , CM000663.1:g.161559423C>T | GRCh37 |
NC_000001.9:g.159826047C>T | NCBI36 |
NG_011982.1:g.13295C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699402.1:c.41-40602G>A | ENSP00000514363.1:n.41-40602G>A | |
ENST00000699403.1:c.61+40735G>A | ENSP00000514364.1:n.61+40735G>A | |
ENST00000465075.6:n.297C>T | ||
ENST00000466542.6:c.205C>T | ENSP00000426627.1:p.Leu69= | |
ENST00000473530.6:n.386C>T | ||
ENST00000473712.6:n.227C>T | ||
ENST00000482226.2:n.184C>T | ||
ENST00000496692.6:n.301C>T | ||
ENST00000502411.5:n.502C>T | ||
ENST00000543859.5:c.202C>T | ENSP00000444663.2:p.Leu68= | |
ENST00000611236.1:c.202C>T | ENSP00000480953.1:p.Leu68= | |
NR_047648.1:n.304C>T |