Canonical Allele Identifier: CA2033475776

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852791G= , CM000674.2:g.45852791G=	GRCh38
NC_000012.11:g.46246574G= , CM000674.1:g.46246574G=	GRCh37
NC_000012.10:g.44532841G=	NCBI36
NG_052800.1:g.128127G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4668G=	ENSP00000415650.3:p.Val1556=
ENST00000457135.2:c.877G=
ENST00000334344.11:c.4668G= MANE Select	ENSP00000335044.6:p.Val1556=
ENST00000422737.6:c.4589G=
ENST00000334344.10:c.4668G=	ENSP00000335044.6:p.Val1556=
ENST00000422737.5:c.4221G=	ENSP00000415650.1:p.Val1407=
ENST00000444670.5:c.3498G=	ENSP00000397307.1:p.Val1166=
ENST00000457135.1:c.492G=	ENSP00000388357.1:p.Val164=
ENST00000479608.5:n.3959G=
NM_152641.2:c.4668G=	NP_689854.2:p.Val1556=
XM_006719272.2:c.4668G=	XP_006719335.1:p.Val1556=
XM_011538025.1:c.3036G=	XP_011536327.1:p.Val1012=
XR_944505.1:n.4816G=
NM_001347839.1:c.4668G=	NP_001334768.1:p.Val1556=
NM_152641.3:c.4668G=	NP_689854.2:p.Val1556=
XM_006719272.4:c.4668G=	XP_006719335.1:p.Val1556=
XR_944505.3:n.4799G=
NM_152641.4:c.4668G= MANE Select	NP_689854.2:p.Val1556=
NM_001347839.2:c.4668G=	NP_001334768.1:p.Val1556=