Canonical Allele Identifier: CA393625287

Gene: ARNT2

Linked Data

• MyVariant Identifiers: chr15:g.80884010T>G (hg19) ; chr15:g.80591669T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80591669T>G , CM000677.2:g.80591669T>G	GRCh38
NC_000015.9:g.80884010T>G , CM000677.1:g.80884010T>G	GRCh37
NC_000015.8:g.78671065T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.2020T>G MANE Select	ENSP00000307479.4:p.Ser674Ala
ENST00000303329.8:c.2020T>G	ENSP00000307479.4:p.Ser674Ala
ENST00000527771.5:c.1987T>G	ENSP00000453792.1:p.Ser663Ala
ENST00000533983.5:c.1987T>G	ENSP00000453651.1:p.Ser663Ala
ENST00000610490.4:c.*318T>G	ENSP00000483762.1:n.*318T>G
ENST00000622346.4:c.2020T>G	ENSP00000479393.1:p.Ser674Ala
NM_014862.3:c.2020T>G	NP_055677.3:p.Ser674Ala
NM_014862.4:c.2020T>G MANE Select	NP_055677.3:p.Ser674Ala