Canonical Allele Identifier: CA2439980714

Gene: TBX22

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026634G= , CM000685.2:g.80026634G=	GRCh38
NC_000023.10:g.79282133G= , CM000685.1:g.79282133G=	GRCh37
NC_000023.9:g.79168789G=	NCBI36
NG_008998.1:g.16879G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373296.8:c.634-70G= MANE Select	ENSP00000362393.3:n.634-70G=
ENST00000373294.8:c.634-70G=	ENSP00000362390.5:n.634-70G=
ENST00000373296.7:c.634-70G=	ENSP00000362393.3:n.634-70G=
ENST00000626498.2:c.*246-70G=	ENSP00000487527.1:n.*246-70G=
ENST00000626877.1:n.513-70G=
NM_001109878.1:c.634-70G=	NP_001103348.1:n.634-70G=
NM_001109879.1:c.274-70G=	NP_001103349.1:n.274-70G=
NM_001303475.1:c.274-70G=	NP_001290404.1:n.274-70G=
NM_016954.2:c.634-70G=	NP_058650.1:n.634-70G=
XM_005262136.2:c.637-70G=	XP_005262193.1:n.637-70G=
XM_006724657.2:c.637-70G=	XP_006724720.1:n.637-70G=
XM_011530972.1:c.274-70G=	XP_011529274.1:n.274-70G=
NM_001109878.2:c.634-70G= MANE Select	NP_001103348.1:n.634-70G=
NM_001109879.2:c.274-70G=	NP_001103349.1:n.274-70G=