Canonical Allele Identifier: CA156903961

Gene: GLI3

Linked Data

• dbSNP Id: rs948927518
• gnomAD v2: 7-42005204-G-A
• gnomAD v3: 7-41965606-G-A
• gnomAD v4: 7-41965606-G-A
• MyVariant Identifiers: chr7:g.42005204G>A (hg19) ; chr7:g.41965606G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41965606G>A , CM000669.2:g.41965606G>A	GRCh38
NC_000007.13:g.42005204G>A , CM000669.1:g.42005204G>A	GRCh37
NC_000007.12:g.41971729G>A	NCBI36
NG_008434.1:g.276415C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.3467C>T MANE Select	ENSP00000379258.3:p.Thr1156Ile
ENST00000677288.1:c.3293C>T	ENSP00000503986.1:p.Thr1098Ile
ENST00000677605.1:c.3467C>T	ENSP00000503743.1:p.Thr1156Ile
ENST00000678429.1:c.3467C>T	ENSP00000502957.1:p.Thr1156Ile
ENST00000395925.7:c.3467C>T	ENSP00000379258.3:p.Thr1156Ile
ENST00000479210.1:n.3444C>T
NM_000168.5:c.3467C>T	NP_000159.3:p.Thr1156Ile
XM_005249703.1:c.3467C>T	XP_005249760.1:p.Thr1156Ile
XM_005249704.2:c.3467C>T	XP_005249761.1:p.Thr1156Ile
XM_011515272.1:c.3467C>T	XP_011513574.1:p.Thr1156Ile
XM_011515273.1:c.3467C>T	XP_011513575.1:p.Thr1156Ile
XM_011515274.1:c.3290C>T	XP_011513576.1:p.Thr1097Ile
XM_011515274.2:c.3290C>T	XP_011513576.1:p.Thr1097Ile
XM_017011997.1:c.3464C>T	XP_016867486.1:p.Thr1155Ile
NM_000168.6:c.3467C>T MANE Select	NP_000159.3:p.Thr1156Ile