Canonical Allele Identifier: CA7692246
Gene: ARNT2 HGNC NCBI

Linked Data

dbSNP Id: rs755331964

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591695A>G , CM000677.2:g.80591695A>G GRCh38
NC_000015.9:g.80884036A>G , CM000677.1:g.80884036A>G GRCh37
NC_000015.8:g.78671091A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.2046A>G MANE Select ENSP00000307479.4:p.Glu682=
ENST00000303329.8:c.2046A>G ENSP00000307479.4:p.Glu682=
ENST00000527771.5:c.2013A>G ENSP00000453792.1:p.Glu671=
ENST00000533983.5:c.2013A>G ENSP00000453651.1:p.Glu671=
ENST00000610490.4:c.*344A>G ENSP00000483762.1:n.*344A>G
ENST00000622346.4:c.2046A>G ENSP00000479393.1:p.Glu682=
NM_014862.3:c.2046A>G NP_055677.3:p.Glu682=
NM_014862.4:c.2046A>G MANE Select NP_055677.3:p.Glu682=