Canonical Allele Identifier: CA10654382

Gene: TBX22

Linked Data

• ClinVar Variation Id: 368661
• ClinVar RCV Id: RCV000399140 ; RCV003437158
• dbSNP Id: rs746947861
• gnomAD v2: X-79270361-G-A
• gnomAD v3: X-80014862-G-A
• gnomAD v4: X-80014862-G-A
• MyVariant Identifiers: chrX:g.79270361G>A (hg19) ; chrX:g.80014862G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80014862G>A , CM000685.2:g.80014862G>A	GRCh38
NC_000023.10:g.79270361G>A , CM000685.1:g.79270361G>A	GRCh37
NC_000023.9:g.79157017G>A	NCBI36
NG_008998.1:g.5107G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.-28G>A MANE Select	ENSP00000362393.3:n.-28G>A
ENST00000373296.7:c.-28G>A	ENSP00000362393.3:n.-28G>A
ENST00000476373.1:n.94G>A
ENST00000626498.2:c.-28G>A	ENSP00000487527.1:n.-28G>A
NM_001109878.1:c.-28G>A	NP_001103348.1:n.-28G>A
NM_001109879.1:c.-384G>A	NP_001103349.1:n.-384G>A
XM_005262136.2:c.-28G>A	XP_005262193.1:n.-28G>A
XM_006724657.2:c.-28G>A	XP_006724720.1:n.-28G>A
XM_011530972.1:c.-1066G>A	XP_011529274.1:n.-1066G>A
NM_001109878.2:c.-28G>A MANE Select	NP_001103348.1:n.-28G>A
NM_001109879.2:c.-384G>A	NP_001103349.1:n.-384G>A