Canonical Allele Identifier: CA4231012

Gene: GLI3

Linked Data

• ClinVar Variation Id: 2074240
• ClinVar RCV Id: RCV002976113
• dbSNP Id: rs749466789
• ExAC: 7:42079709 G / A
• gnomAD v2: 7-42079709-G-A
• gnomAD v4: 7-42040110-G-A
• MyVariant Identifiers: chr7:g.42079709G>A (hg19) ; chr7:g.42040110G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42040110G>A , CM000669.2:g.42040110G>A	GRCh38
NC_000007.13:g.42079709G>A , CM000669.1:g.42079709G>A	GRCh37
NC_000007.12:g.42046234G>A	NCBI36
NG_008434.1:g.201910C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.956C>T MANE Select	ENSP00000379258.3:p.Thr319Met
ENST00000677288.1:c.779C>T	ENSP00000503986.1:p.Thr260Met
ENST00000677605.1:c.956C>T	ENSP00000503743.1:p.Thr319Met
ENST00000678429.1:c.956C>T	ENSP00000502957.1:p.Thr319Met
ENST00000395925.7:c.956C>T	ENSP00000379258.3:p.Thr319Met
ENST00000479210.1:n.933C>T
NM_000168.5:c.956C>T	NP_000159.3:p.Thr319Met
XM_005249703.1:c.956C>T	XP_005249760.1:p.Thr319Met
XM_005249704.2:c.956C>T	XP_005249761.1:p.Thr319Met
XM_011515272.1:c.956C>T	XP_011513574.1:p.Thr319Met
XM_011515273.1:c.956C>T	XP_011513575.1:p.Thr319Met
XM_011515274.1:c.779C>T	XP_011513576.1:p.Thr260Met
XM_011515274.2:c.779C>T	XP_011513576.1:p.Thr260Met
XM_017011997.1:c.953C>T	XP_016867486.1:p.Thr318Met
NM_000168.6:c.956C>T MANE Select	NP_000159.3:p.Thr319Met