Canonical Allele Identifier: CA2190489665

Gene: ARNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80591623G= , CM000677.2:g.80591623G=	GRCh38
NC_000015.9:g.80883964G= , CM000677.1:g.80883964G=	GRCh37
NC_000015.8:g.78671019G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.1974G= MANE Select	ENSP00000307479.4:p.Ser658=
ENST00000303329.8:c.1974G=	ENSP00000307479.4:p.Ser658=
ENST00000527771.5:c.1941G=	ENSP00000453792.1:p.Ser647=
ENST00000533983.5:c.1941G=	ENSP00000453651.1:p.Ser647=
ENST00000610490.4:c.*272G=	ENSP00000483762.1:n.*272G=
ENST00000622346.4:c.1974G=	ENSP00000479393.1:p.Ser658=
NM_014862.3:c.1974G=	NP_055677.3:p.Ser658=
NM_014862.4:c.1974G= MANE Select	NP_055677.3:p.Ser658=