Canonical Allele Identifier: CA1851397
Gene: GLI2 HGNC NCBI

Linked Data

ClinVar Variation Id: 419104
dbSNP Id: rs201053024

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120797408A>C , CM000664.2:g.120797408A>C GRCh38
NC_000002.11:g.121554984A>C , CM000664.1:g.121554984A>C GRCh37
NC_000002.10:g.121271454A>C NCBI36
NG_009030.1:g.5118A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.88A>C MANE Select ENSP00000354586.5:p.Lys30Gln
ENST00000418323.6:c.88A>C ENSP00000398992.1:p.Lys30Gln
ENST00000452319.6:c.88A>C ENSP00000390436.1:p.Lys30Gln
ENST00000482119.6:c.88A>C ENSP00000502423.1:p.Lys30Gln
ENST00000314490.15:c.-200A>C ENSP00000312694.12:n.-200A>C
ENST00000341310.10:c.88A>C ENSP00000344473.6:p.Lys30Gln
ENST00000360874.10:c.64A>C ENSP00000441454.1:p.Lys22Gln
ENST00000361492.8:c.88A>C ENSP00000354586.4:p.Lys30Gln
ENST00000418323.5:c.88A>C ENSP00000398992.1:p.Lys30Gln
ENST00000433812.1:c.64A>C ENSP00000402383.1:p.Lys22Gln
ENST00000435313.6:n.113A>C
ENST00000437950.5:c.88A>C ENSP00000415773.1:p.Lys30Gln
ENST00000438299.5:c.88A>C ENSP00000400593.1:p.Lys30Gln
ENST00000445186.5:c.88A>C ENSP00000397488.1:p.Lys30Gln
ENST00000452319.5:c.88A>C ENSP00000390436.1:p.Lys30Gln
ENST00000452692.5:c.88A>C ENSP00000403715.1:p.Lys30Gln
ENST00000472722.5:n.177A>C
ENST00000482119.5:n.177A>C
NM_005270.4:c.88A>C NP_005261.2:p.Lys30Gln
XM_006712422.1:c.88A>C XP_006712485.1:p.Lys30Gln
XM_011510974.1:c.-182A>C XP_011509276.1:n.-182A>C
XM_006712422.3:c.88A>C XP_006712485.1:p.Lys30Gln
XM_011510973.2:c.-182A>C XP_011509275.1:n.-182A>C
XM_011510974.2:c.-182A>C XP_011509276.1:n.-182A>C
XM_024452794.1:c.88A>C XP_024308562.1:p.Lys30Gln
XM_024452795.1:c.88A>C XP_024308563.1:p.Lys30Gln
NM_001371271.1:c.88A>C NP_001358200.1:p.Lys30Gln
NM_001374353.1:c.88A>C MANE Select NP_001361282.1:p.Lys30Gln
NM_001374354.1:c.-182A>C NP_001361283.1:n.-182A>C
NM_005270.5:c.88A>C NP_005261.2:p.Lys30Gln