Canonical Allele Identifier: CA413740612

Gene: TBX22

Linked Data

• MyVariant Identifiers: chrX:g.79282204T>G (hg19) ; chrX:g.80026705T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.635T>G MANE Select	ENSP00000362393.3:p.Ile212Ser
ENST00000373294.8:c.635T>G	ENSP00000362390.5:p.Ile212Ser
ENST00000373296.7:c.635T>G	ENSP00000362393.3:p.Ile212Ser
ENST00000626498.2:c.*247T>G	ENSP00000487527.1:n.*247T>G
ENST00000626877.1:n.514T>G
NM_001109878.1:c.635T>G	NP_001103348.1:p.Ile212Ser
NM_001109879.1:c.275T>G	NP_001103349.1:p.Ile92Ser
NM_001303475.1:c.275T>G	NP_001290404.1:p.Ile92Ser
NM_016954.2:c.635T>G	NP_058650.1:p.Ile212Ser
XM_005262136.2:c.638T>G	XP_005262193.1:p.Ile213Ser
XM_006724657.2:c.638T>G	XP_006724720.1:p.Ile213Ser
XM_011530972.1:c.275T>G	XP_011529274.1:p.Ile92Ser
NM_001109878.2:c.635T>G MANE Select	NP_001103348.1:p.Ile212Ser
NM_001109879.2:c.275T>G	NP_001103349.1:p.Ile92Ser