Canonical Allele Identifier: CA348173098

Gene: GLI2

Linked Data

• MyVariant Identifiers: chr2:g.121746753C>G (hg19) ; chr2:g.120989177C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120989177C>G , CM000664.2:g.120989177C>G	GRCh38
NC_000002.11:g.121746753C>G , CM000664.1:g.121746753C>G	GRCh37
NC_000002.10:g.121463223C>G	NCBI36
NG_009030.1:g.196887C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361492.9:c.3212C>G MANE Select	ENSP00000354586.5:p.Thr1071Arg
ENST00000452319.6:c.3263C>G	ENSP00000390436.1:p.Thr1088Arg
ENST00000341310.10:c.*2311C>G	ENSP00000344473.6:n.*2311C>G
ENST00000361492.8:c.3263C>G	ENSP00000354586.4:p.Thr1088Arg
ENST00000438299.5:c.*2362C>G	ENSP00000400593.1:n.*2362C>G
ENST00000445186.5:c.*2362C>G	ENSP00000397488.1:n.*2362C>G
ENST00000452319.5:c.3263C>G	ENSP00000390436.1:p.Thr1088Arg
ENST00000452692.5:c.*2311C>G	ENSP00000403715.1:n.*2311C>G
NM_005270.4:c.3263C>G	NP_005261.2:p.Thr1088Arg
XM_006712422.1:c.3212C>G	XP_006712485.1:p.Thr1071Arg
XM_011510969.1:c.3245C>G	XP_011509271.1:p.Thr1082Arg
XM_011510970.1:c.3122C>G	XP_011509272.1:p.Thr1041Arg
XM_011510971.1:c.3068C>G	XP_011509273.1:p.Thr1023Arg
XM_011510972.1:c.3068C>G	XP_011509274.1:p.Thr1023Arg
XM_011510973.1:c.2888C>G	XP_011509275.1:p.Thr963Arg
XM_011510974.1:c.2837C>G	XP_011509276.1:p.Thr946Arg
XM_006712422.3:c.3212C>G	XP_006712485.1:p.Thr1071Arg
XM_011510969.2:c.3515C>G	XP_011509271.2:p.Thr1172Arg
XM_011510970.2:c.3122C>G	XP_011509272.1:p.Thr1041Arg
XM_011510971.2:c.3068C>G	XP_011509273.1:p.Thr1023Arg
XM_011510972.2:c.3164C>G	XP_011509274.2:p.Thr1055Arg
XM_011510973.2:c.2888C>G	XP_011509275.1:p.Thr963Arg
XM_011510974.2:c.2837C>G	XP_011509276.1:p.Thr946Arg
XM_017003818.1:c.3464C>G	XP_016859307.1:p.Thr1155Arg
XM_024452794.1:c.3263C>G	XP_024308562.1:p.Thr1088Arg
XM_024452795.1:c.3263C>G	XP_024308563.1:p.Thr1088Arg
NM_001371271.1:c.3263C>G	NP_001358200.1:p.Thr1088Arg
NM_001374353.1:c.3212C>G MANE Select	NP_001361282.1:p.Thr1071Arg
NM_001374354.1:c.2837C>G	NP_001361283.1:p.Thr946Arg
NM_005270.5:c.3263C>G	NP_005261.2:p.Thr1088Arg