Canonical Allele Identifier: CA2694191469

Gene: TBX22

Linked Data

• gnomAD v4: X-80025595-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80025595T>C , CM000685.2:g.80025595T>C	GRCh38
NC_000023.10:g.79281094T>C , CM000685.1:g.79281094T>C	GRCh37
NC_000023.9:g.79167750T>C	NCBI36
NG_008998.1:g.15840T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.459-8T>C MANE Select	ENSP00000362393.3:n.459-8T>C
ENST00000373294.8:c.459-8T>C	ENSP00000362390.5:n.459-8T>C
ENST00000373296.7:c.459-8T>C	ENSP00000362393.3:n.459-8T>C
ENST00000626498.2:c.*71-8T>C	ENSP00000487527.1:n.*71-8T>C
ENST00000626877.1:n.338-8T>C
NM_001109878.1:c.459-8T>C	NP_001103348.1:n.459-8T>C
NM_001109879.1:c.99-8T>C	NP_001103349.1:n.99-8T>C
NM_001303475.1:c.99-8T>C	NP_001290404.1:n.99-8T>C
NM_016954.2:c.459-8T>C	NP_058650.1:n.459-8T>C
XM_005262136.2:c.462-8T>C	XP_005262193.1:n.462-8T>C
XM_006724657.2:c.462-8T>C	XP_006724720.1:n.462-8T>C
XM_011530972.1:c.99-8T>C	XP_011529274.1:n.99-8T>C
NM_001109878.2:c.459-8T>C MANE Select	NP_001103348.1:n.459-8T>C
NM_001109879.2:c.99-8T>C	NP_001103349.1:n.99-8T>C