Canonical Allele Identifier: CA413740303
Gene: TBX22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.80025650A>G , CM000685.2:g.80025650A>G GRCh38
NC_000023.10:g.79281149A>G , CM000685.1:g.79281149A>G GRCh37
NC_000023.9:g.79167805A>G NCBI36
NG_008998.1:g.15895A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373296.8:c.506A>G MANE Select ENSP00000362393.3:p.His169Arg
ENST00000373294.8:c.506A>G ENSP00000362390.5:p.His169Arg
ENST00000373296.7:c.506A>G ENSP00000362393.3:p.His169Arg
ENST00000626498.2:c.*118A>G ENSP00000487527.1:n.*118A>G
ENST00000626877.1:n.385A>G
NM_001109878.1:c.506A>G NP_001103348.1:p.His169Arg
NM_001109879.1:c.146A>G NP_001103349.1:p.His49Arg
NM_001303475.1:c.146A>G NP_001290404.1:p.His49Arg
NM_016954.2:c.506A>G NP_058650.1:p.His169Arg
XM_005262136.2:c.509A>G XP_005262193.1:p.His170Arg
XM_006724657.2:c.509A>G XP_006724720.1:p.His170Arg
XM_011530972.1:c.146A>G XP_011529274.1:p.His49Arg
NM_001109878.2:c.506A>G MANE Select NP_001103348.1:p.His169Arg
NM_001109879.2:c.146A>G NP_001103349.1:p.His49Arg