Canonical Allele Identifier: CA2694191627

Gene: TBX22

Linked Data

• gnomAD v4: X-80026646-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026646A>G , CM000685.2:g.80026646A>G	GRCh38
NC_000023.10:g.79282145A>G , CM000685.1:g.79282145A>G	GRCh37
NC_000023.9:g.79168801A>G	NCBI36
NG_008998.1:g.16891A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.634-58A>G MANE Select	ENSP00000362393.3:n.634-58A>G
ENST00000373294.8:c.634-58A>G	ENSP00000362390.5:n.634-58A>G
ENST00000373296.7:c.634-58A>G	ENSP00000362393.3:n.634-58A>G
ENST00000626498.2:c.*246-58A>G	ENSP00000487527.1:n.*246-58A>G
ENST00000626877.1:n.513-58A>G
NM_001109878.1:c.634-58A>G	NP_001103348.1:n.634-58A>G
NM_001109879.1:c.274-58A>G	NP_001103349.1:n.274-58A>G
NM_001303475.1:c.274-58A>G	NP_001290404.1:n.274-58A>G
NM_016954.2:c.634-58A>G	NP_058650.1:n.634-58A>G
XM_005262136.2:c.637-58A>G	XP_005262193.1:n.637-58A>G
XM_006724657.2:c.637-58A>G	XP_006724720.1:n.637-58A>G
XM_011530972.1:c.274-58A>G	XP_011529274.1:n.274-58A>G
NM_001109878.2:c.634-58A>G MANE Select	NP_001103348.1:n.634-58A>G
NM_001109879.2:c.274-58A>G	NP_001103349.1:n.274-58A>G