Canonical Allele Identifier: CA121424
Gene: TBX22 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11330
ClinVar RCV Id: RCV000012083
dbSNP Id: rs104894944

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.80023236G>T , CM000685.2:g.80023236G>T GRCh38
NC_000023.10:g.79278735G>T , CM000685.1:g.79278735G>T GRCh37
NC_000023.9:g.79165391G>T NCBI36
NG_008998.1:g.13481G>T

Transcript Alleles

HGVS Amino-acid change
NM_001109878.1:c.352G>T VV NP_001103348.1:p.Gly118Cys
NM_001109879.1:c.-5G>T VV NP_001103349.1:p.=
NM_001303475.1:c.-72G>T VV NP_001290404.1:p.=
NM_016954.2:c.352G>T VV NP_058650.1:p.Gly118Cys
XM_005262136.2:c.355G>T XP_005262193.1:p.Gly119Cys
XM_006724657.2:c.355G>T XP_006724720.1:p.Gly119Cys
XM_011530972.1:c.-72G>T XP_011529274.1:p.=
NM_001109878.2:c.352G>T VV MANE Preferred
ENST00000373294.8:c.352G>T ENSP00000362390.5:p.Gly118Cys
ENST00000373296.7:c.352G>T ENSP00000362393.3:p.Gly118Cys
ENST00000626498.2:c.352G>T ENSP00000487527.1:p.Gly118Cys
ENST00000626877.1:n.168G>T