Canonical Allele Identifier: CA156899220

Gene: GLI3

Linked Data

• ClinVar Variation Id: 908612
• ClinVar RCV Id: RCV001159183 ; RCV001159184
• dbSNP Id: rs865942966
• gnomAD v3: 7-41962241-C-T
• gnomAD v4: 7-41962241-C-T
• MyVariant Identifiers: chr7:g.42001839C>T (hg19) ; chr7:g.41962241C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41962241C>T , CM000669.2:g.41962241C>T	GRCh38
NC_000007.13:g.42001839C>T , CM000669.1:g.42001839C>T	GRCh37
NC_000007.12:g.41968364C>T	NCBI36
NG_008434.1:g.279780G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.*2089G>A MANE Select	ENSP00000379258.3:n.*2089G>A
ENST00000677288.1:c.*2089G>A	ENSP00000503986.1:n.*2089G>A
ENST00000677605.1:c.*2089G>A	ENSP00000503743.1:n.*2089G>A
ENST00000678429.1:c.*2089G>A	ENSP00000502957.1:n.*2089G>A
ENST00000395925.7:c.*2089G>A	ENSP00000379258.3:n.*2089G>A
NM_000168.5:c.*2089G>A	NP_000159.3:n.*2089G>A
XM_005249703.1:c.*2089G>A	XP_005249760.1:n.*2089G>A
XM_005249704.2:c.*2089G>A	XP_005249761.1:n.*2089G>A
XM_011515272.1:c.*2089G>A	XP_011513574.1:n.*2089G>A
XM_011515273.1:c.*2089G>A	XP_011513575.1:n.*2089G>A
XM_011515274.1:c.*2089G>A	XP_011513576.1:n.*2089G>A
NM_000168.6:c.*2089G>A MANE Select	NP_000159.3:n.*2089G>A