Canonical Allele Identifier: CA716113213

Gene: ARNT2

Linked Data

• dbSNP Id: rs1287591057
• gnomAD v3: 15-80451424-G-A
• gnomAD v4: 15-80451424-G-A
• MyVariant Identifiers: chr15:g.80743765G>A (hg19) ; chr15:g.80451424G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80451424G>A , CM000677.2:g.80451424G>A	GRCh38
NC_000015.9:g.80743765G>A , CM000677.1:g.80743765G>A	GRCh37
NC_000015.8:g.78530820G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.146+430G>A MANE Select	ENSP00000307479.4:n.146+430G>A
ENST00000303329.8:c.146+430G>A	ENSP00000307479.4:n.146+430G>A
ENST00000525103.1:c.-57+10046G>A	ENSP00000452961.1:n.-57+10046G>A
ENST00000527771.5:c.113+430G>A	ENSP00000453792.1:n.113+430G>A
ENST00000529181.1:n.312+430G>A
ENST00000533983.5:c.113+430G>A	ENSP00000453651.1:n.113+430G>A
ENST00000610490.4:c.146+430G>A	ENSP00000483762.1:n.146+430G>A
ENST00000622346.4:c.146+430G>A	ENSP00000479393.1:n.146+430G>A
NM_014862.3:c.146+430G>A	NP_055677.3:n.146+430G>A
NM_014862.4:c.146+430G>A MANE Select	NP_055677.3:n.146+430G>A