Canonical Allele Identifier: CA2439979097

Gene: TBX22

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80022435G= , CM000685.2:g.80022435G=	GRCh38
NC_000023.10:g.79277934G= , CM000685.1:g.79277934G=	GRCh37
NC_000023.9:g.79164590G=	NCBI36
NG_008998.1:g.12680G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.166G= MANE Select	ENSP00000362393.3:p.Glu56=
ENST00000373294.8:c.166G=	ENSP00000362390.5:p.Glu56=
ENST00000373296.7:c.166G=	ENSP00000362393.3:p.Glu56=
ENST00000476373.1:n.287G=
ENST00000626498.2:c.166G=	ENSP00000487527.1:p.Glu56=
NM_001109878.1:c.166G=	NP_001103348.1:p.Glu56=
NM_001109879.1:c.-191G=	NP_001103349.1:n.-191G=
NM_016954.2:c.166G=	NP_058650.1:p.Glu56=
XM_005262136.2:c.166G=	XP_005262193.1:p.Glu56=
XM_006724657.2:c.166G=	XP_006724720.1:p.Glu56=
XM_011530972.1:c.-873G=	XP_011529274.1:n.-873G=
NM_001109878.2:c.166G= MANE Select	NP_001103348.1:p.Glu56=
NM_001109879.2:c.-191G=	NP_001103349.1:n.-191G=