Canonical Allele Identifier: CA2190457926

Gene: ARNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80451533G= , CM000677.2:g.80451533G=	GRCh38
NC_000015.9:g.80743874G= , CM000677.1:g.80743874G=	GRCh37
NC_000015.8:g.78530929G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.146+539G= MANE Select	ENSP00000307479.4:n.146+539G=
ENST00000303329.8:c.146+539G=	ENSP00000307479.4:n.146+539G=
ENST00000525103.1:c.-57+10155G=	ENSP00000452961.1:n.-57+10155G=
ENST00000527771.5:c.113+539G=	ENSP00000453792.1:n.113+539G=
ENST00000529181.1:n.312+539G=
ENST00000533983.5:c.113+539G=	ENSP00000453651.1:n.113+539G=
ENST00000610490.4:c.146+539G=	ENSP00000483762.1:n.146+539G=
ENST00000622346.4:c.146+539G=	ENSP00000479393.1:n.146+539G=
NM_014862.3:c.146+539G=	NP_055677.3:n.146+539G=
NM_014862.4:c.146+539G= MANE Select	NP_055677.3:n.146+539G=