Canonical Allele Identifier: CA393624764

Gene: ARNT2

Linked Data

• MyVariant Identifiers: chr15:g.80883942G>T (hg19) ; chr15:g.80591601G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80591601G>T , CM000677.2:g.80591601G>T	GRCh38
NC_000015.9:g.80883942G>T , CM000677.1:g.80883942G>T	GRCh37
NC_000015.8:g.78670997G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.1952G>T MANE Select	ENSP00000307479.4:p.Gly651Val
ENST00000303329.8:c.1952G>T	ENSP00000307479.4:p.Gly651Val
ENST00000527771.5:c.1919G>T	ENSP00000453792.1:p.Gly640Val
ENST00000533983.5:c.1919G>T	ENSP00000453651.1:p.Gly640Val
ENST00000610490.4:c.*250G>T	ENSP00000483762.1:n.*250G>T
ENST00000622346.4:c.1952G>T	ENSP00000479393.1:p.Gly651Val
NM_014862.3:c.1952G>T	NP_055677.3:p.Gly651Val
NM_014862.4:c.1952G>T MANE Select	NP_055677.3:p.Gly651Val