Canonical Allele Identifier: CA413740620

Gene: TBX22

Linked Data

• MyVariant Identifiers: chrX:g.79282207T>C (hg19) ; chrX:g.80026708T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026708T>C , CM000685.2:g.80026708T>C	GRCh38
NC_000023.10:g.79282207T>C , CM000685.1:g.79282207T>C	GRCh37
NC_000023.9:g.79168863T>C	NCBI36
NG_008998.1:g.16953T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.638T>C MANE Select	ENSP00000362393.3:p.Ile213Thr
ENST00000373294.8:c.638T>C	ENSP00000362390.5:p.Ile213Thr
ENST00000373296.7:c.638T>C	ENSP00000362393.3:p.Ile213Thr
ENST00000626498.2:c.*250T>C	ENSP00000487527.1:n.*250T>C
ENST00000626877.1:n.517T>C
NM_001109878.1:c.638T>C	NP_001103348.1:p.Ile213Thr
NM_001109879.1:c.278T>C	NP_001103349.1:p.Ile93Thr
NM_001303475.1:c.278T>C	NP_001290404.1:p.Ile93Thr
NM_016954.2:c.638T>C	NP_058650.1:p.Ile213Thr
XM_005262136.2:c.641T>C	XP_005262193.1:p.Ile214Thr
XM_006724657.2:c.641T>C	XP_006724720.1:p.Ile214Thr
XM_011530972.1:c.278T>C	XP_011529274.1:p.Ile93Thr
NM_001109878.2:c.638T>C MANE Select	NP_001103348.1:p.Ile213Thr
NM_001109879.2:c.278T>C	NP_001103349.1:p.Ile93Thr