Canonical Allele Identifier: CA274319185

Gene: ARNT2

Linked Data

• dbSNP Id: rs1045363083
• MyVariant Identifiers: chr15:g.80743949G>A (hg19) ; chr15:g.80451608G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80451608G>A , CM000677.2:g.80451608G>A	GRCh38
NC_000015.9:g.80743949G>A , CM000677.1:g.80743949G>A	GRCh37
NC_000015.8:g.78531004G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.146+614G>A MANE Select	ENSP00000307479.4:n.146+614G>A
ENST00000303329.8:c.146+614G>A	ENSP00000307479.4:n.146+614G>A
ENST00000525103.1:c.-57+10230G>A	ENSP00000452961.1:n.-57+10230G>A
ENST00000527771.5:c.113+614G>A	ENSP00000453792.1:n.113+614G>A
ENST00000529181.1:n.312+614G>A
ENST00000533983.5:c.113+614G>A	ENSP00000453651.1:n.113+614G>A
ENST00000610490.4:c.146+614G>A	ENSP00000483762.1:n.146+614G>A
ENST00000622346.4:c.146+614G>A	ENSP00000479393.1:n.146+614G>A
NM_014862.3:c.146+614G>A	NP_055677.3:n.146+614G>A
NM_014862.4:c.146+614G>A MANE Select	NP_055677.3:n.146+614G>A