Canonical Allele Identifier: CA367320707

Gene: GLI3

Linked Data

• ClinVar Variation Id: 2572670
• ClinVar RCV Id: RCV003314784
• dbSNP Id: rs1787187346
• gnomAD v3: 7-41966458-G-C
• gnomAD v4: 7-41966458-G-C
• MyVariant Identifiers: chr7:g.42006056G>C (hg19) ; chr7:g.41966458G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41966458G>C , CM000669.2:g.41966458G>C	GRCh38
NC_000007.13:g.42006056G>C , CM000669.1:g.42006056G>C	GRCh37
NC_000007.12:g.41972581G>C	NCBI36
NG_008434.1:g.275563C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.2615C>G MANE Select	ENSP00000379258.3:p.Ser872Cys
ENST00000677288.1:c.2441C>G	ENSP00000503986.1:p.Ser814Cys
ENST00000677605.1:c.2615C>G	ENSP00000503743.1:p.Ser872Cys
ENST00000678429.1:c.2615C>G	ENSP00000502957.1:p.Ser872Cys
ENST00000395925.7:c.2615C>G	ENSP00000379258.3:p.Ser872Cys
ENST00000479210.1:n.2592C>G
NM_000168.5:c.2615C>G	NP_000159.3:p.Ser872Cys
XM_005249703.1:c.2615C>G	XP_005249760.1:p.Ser872Cys
XM_005249704.2:c.2615C>G	XP_005249761.1:p.Ser872Cys
XM_011515272.1:c.2615C>G	XP_011513574.1:p.Ser872Cys
XM_011515273.1:c.2615C>G	XP_011513575.1:p.Ser872Cys
XM_011515274.1:c.2438C>G	XP_011513576.1:p.Ser813Cys
XM_011515274.2:c.2438C>G	XP_011513576.1:p.Ser813Cys
XM_017011997.1:c.2612C>G	XP_016867486.1:p.Ser871Cys
NM_000168.6:c.2615C>G MANE Select	NP_000159.3:p.Ser872Cys