Canonical Allele Identifier: CA413740614
Gene: TBX22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.80026705T>C , CM000685.2:g.80026705T>C GRCh38
NC_000023.10:g.79282204T>C , CM000685.1:g.79282204T>C GRCh37
NC_000023.9:g.79168860T>C NCBI36
NG_008998.1:g.16950T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373296.8:c.635T>C MANE Select ENSP00000362393.3:p.Ile212Thr
ENST00000373294.8:c.635T>C ENSP00000362390.5:p.Ile212Thr
ENST00000373296.7:c.635T>C ENSP00000362393.3:p.Ile212Thr
ENST00000626498.2:c.*247T>C ENSP00000487527.1:n.*247T>C
ENST00000626877.1:n.514T>C
NM_001109878.1:c.635T>C NP_001103348.1:p.Ile212Thr
NM_001109879.1:c.275T>C NP_001103349.1:p.Ile92Thr
NM_001303475.1:c.275T>C NP_001290404.1:p.Ile92Thr
NM_016954.2:c.635T>C NP_058650.1:p.Ile212Thr
XM_005262136.2:c.638T>C XP_005262193.1:p.Ile213Thr
XM_006724657.2:c.638T>C XP_006724720.1:p.Ile213Thr
XM_011530972.1:c.275T>C XP_011529274.1:p.Ile92Thr
NM_001109878.2:c.635T>C MANE Select NP_001103348.1:p.Ile212Thr
NM_001109879.2:c.275T>C NP_001103349.1:p.Ile92Thr