Canonical Allele Identifier: CA1702731503

Gene: GLI3

Linked Data

• dbSNP Id: rs1272091387

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42148070G>C , CM000669.2:g.42148070G>C	GRCh38
NC_000007.13:g.42187669G>C , CM000669.1:g.42187669G>C	GRCh37
NC_000007.12:g.42154194G>C	NCBI36
NG_008434.1:g.93950C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.367+156C>G MANE Select	ENSP00000379258.3:n.367+156C>G
ENST00000642432.1:c.190+156C>G	ENSP00000495498.1:n.190+156C>G
ENST00000643264.1:c.190+156C>G	ENSP00000495207.1:n.190+156C>G
ENST00000647255.1:c.190+156C>G	ENSP00000495745.1:n.190+156C>G
ENST00000677288.1:c.190+156C>G	ENSP00000503986.1:n.190+156C>G
ENST00000677605.1:c.367+156C>G	ENSP00000503743.1:n.367+156C>G
ENST00000678429.1:c.367+156C>G	ENSP00000502957.1:n.367+156C>G
ENST00000395925.7:c.367+156C>G	ENSP00000379258.3:n.367+156C>G
ENST00000448703.5:c.367+156C>G	ENSP00000406135.1:n.367+156C>G
ENST00000479210.1:n.344+156C>G
NM_000168.5:c.367+156C>G	NP_000159.3:n.367+156C>G
XM_005249703.1:c.367+156C>G	XP_005249760.1:n.367+156C>G
XM_005249704.2:c.367+156C>G	XP_005249761.1:n.367+156C>G
XM_011515272.1:c.367+156C>G	XP_011513574.1:n.367+156C>G
XM_011515273.1:c.367+156C>G	XP_011513575.1:n.367+156C>G
XM_011515274.1:c.190+156C>G	XP_011513576.1:n.190+156C>G
XM_011515274.2:c.190+156C>G	XP_011513576.1:n.190+156C>G
XM_017011997.1:c.364+156C>G	XP_016867486.1:n.364+156C>G
NM_000168.6:c.367+156C>G MANE Select	NP_000159.3:n.367+156C>G