HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41624273C>T , CM000679.2:g.41624273C>T | GRCh38 |
NC_000017.10:g.39780525C>T , CM000679.1:g.39780525C>T | GRCh37 |
NC_000017.9:g.37034051C>T | NCBI36 |
NG_008625.1:g.5358G>A | |
NG_009090.2:g.167440G>A , LRG_401:g.167440G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311208.13:c.237G>A MANE Select | ENSP00000308452.8:p.Leu79= | |
ENST00000311208.12:c.237G>A | ENSP00000308452.8:p.Leu79= | |
ENST00000463128.5:c.-312-67G>A | ENSP00000468672.1:n.-312-67G>A | |
ENST00000491673.1:n.303G>A | ||
ENST00000493253.5:n.24G>A | ||
ENST00000540235.5:c.32G>A | ENSP00000441751.2:p.Cys11Tyr | |
ENST00000577817.3:c.192G>A | ENSP00000467418.1:p.Leu64= | |
NM_000422.2:c.237G>A | NP_000413.1:p.Leu79= | |
NM_000422.3:c.237G>A MANE Select | NP_000413.1:p.Leu79= |