Canonical Allele Identifier: CA428749753

Gene: GLI2

Linked Data

• MyVariant Identifiers: chr2:g.121746619A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120989043A>T , CM000664.2:g.120989043A>T	GRCh38
NC_000002.11:g.121746619A>T , CM000664.1:g.121746619A>T	GRCh37
NC_000002.10:g.121463089A>T	NCBI36
NG_009030.1:g.196753A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.3078A>T MANE Select	ENSP00000354586.5:p.Gly1026=
ENST00000452319.6:c.3129A>T	ENSP00000390436.1:p.Gly1043=
ENST00000341310.10:c.*2177A>T	ENSP00000344473.6:n.*2177A>T
ENST00000361492.8:c.3129A>T	ENSP00000354586.4:p.Gly1043=
ENST00000438299.5:c.*2228A>T	ENSP00000400593.1:n.*2228A>T
ENST00000445186.5:c.*2228A>T	ENSP00000397488.1:n.*2228A>T
ENST00000452319.5:c.3129A>T	ENSP00000390436.1:p.Gly1043=
ENST00000452692.5:c.*2177A>T	ENSP00000403715.1:n.*2177A>T
NM_005270.4:c.3129A>T	NP_005261.2:p.Gly1043=
XM_006712422.1:c.3078A>T	XP_006712485.1:p.Gly1026=
XM_011510969.1:c.3111A>T	XP_011509271.1:p.Gly1037=
XM_011510970.1:c.2988A>T	XP_011509272.1:p.Gly996=
XM_011510971.1:c.2934A>T	XP_011509273.1:p.Gly978=
XM_011510972.1:c.2934A>T	XP_011509274.1:p.Gly978=
XM_011510973.1:c.2754A>T	XP_011509275.1:p.Gly918=
XM_011510974.1:c.2703A>T	XP_011509276.1:p.Gly901=
XM_006712422.3:c.3078A>T	XP_006712485.1:p.Gly1026=
XM_011510969.2:c.3381A>T	XP_011509271.2:p.Gly1127=
XM_011510970.2:c.2988A>T	XP_011509272.1:p.Gly996=
XM_011510971.2:c.2934A>T	XP_011509273.1:p.Gly978=
XM_011510972.2:c.3030A>T	XP_011509274.2:p.Gly1010=
XM_011510973.2:c.2754A>T	XP_011509275.1:p.Gly918=
XM_011510974.2:c.2703A>T	XP_011509276.1:p.Gly901=
XM_017003818.1:c.3330A>T	XP_016859307.1:p.Gly1110=
XM_024452794.1:c.3129A>T	XP_024308562.1:p.Gly1043=
XM_024452795.1:c.3129A>T	XP_024308563.1:p.Gly1043=
NM_001371271.1:c.3129A>T	NP_001358200.1:p.Gly1043=
NM_001374353.1:c.3078A>T MANE Select	NP_001361282.1:p.Gly1026=
NM_001374354.1:c.2703A>T	NP_001361283.1:p.Gly901=
NM_005270.5:c.3129A>T	NP_005261.2:p.Gly1043=