Canonical Allele Identifier: CA393624787

Gene: ARNT2

Linked Data

• dbSNP Id: rs1471103942
• gnomAD v2: 15-80883955-A-T
• gnomAD v4: 15-80591614-A-T
• MyVariant Identifiers: chr15:g.80883955A>T (hg19) ; chr15:g.80591614A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80591614A>T , CM000677.2:g.80591614A>T	GRCh38
NC_000015.9:g.80883955A>T , CM000677.1:g.80883955A>T	GRCh37
NC_000015.8:g.78671010A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.1965A>T MANE Select	ENSP00000307479.4:p.Glu655Asp
ENST00000303329.8:c.1965A>T	ENSP00000307479.4:p.Glu655Asp
ENST00000527771.5:c.1932A>T	ENSP00000453792.1:p.Glu644Asp
ENST00000533983.5:c.1932A>T	ENSP00000453651.1:p.Glu644Asp
ENST00000610490.4:c.*263A>T	ENSP00000483762.1:n.*263A>T
ENST00000622346.4:c.1965A>T	ENSP00000479393.1:p.Glu655Asp
NM_014862.3:c.1965A>T	NP_055677.3:p.Glu655Asp
NM_014862.4:c.1965A>T MANE Select	NP_055677.3:p.Glu655Asp