Canonical Allele Identifier: CA2190489702

Gene: ARNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80591664A= , CM000677.2:g.80591664A=	GRCh38
NC_000015.9:g.80884005A= , CM000677.1:g.80884005A=	GRCh37
NC_000015.8:g.78671060A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.2015A= MANE Select	ENSP00000307479.4:p.Gln672=
ENST00000303329.8:c.2015A=	ENSP00000307479.4:p.Gln672=
ENST00000527771.5:c.1982A=	ENSP00000453792.1:p.Gln661=
ENST00000533983.5:c.1982A=	ENSP00000453651.1:p.Gln661=
ENST00000610490.4:c.*313A=	ENSP00000483762.1:n.*313A=
ENST00000622346.4:c.2015A=	ENSP00000479393.1:p.Gln672=
NM_014862.3:c.2015A=	NP_055677.3:p.Gln672=
NM_014862.4:c.2015A= MANE Select	NP_055677.3:p.Gln672=