Canonical Allele Identifier: CA971915500

Gene: ARNT2

Linked Data

• dbSNP Id: rs17225178
• gnomAD v3: 15-80451525-T-C
• gnomAD v4: 15-80451525-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80451525T>C , CM000677.2:g.80451525T>C	GRCh38
NC_000015.9:g.80743866T>C , CM000677.1:g.80743866T>C	GRCh37
NC_000015.8:g.78530921T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000303329.9:c.146+531T>C MANE Select	ENSP00000307479.4:n.146+531T>C
ENST00000303329.8:c.146+531T>C	ENSP00000307479.4:n.146+531T>C
ENST00000525103.1:c.-57+10147T>C	ENSP00000452961.1:n.-57+10147T>C
ENST00000527771.5:c.113+531T>C	ENSP00000453792.1:n.113+531T>C
ENST00000529181.1:n.312+531T>C
ENST00000533983.5:c.113+531T>C	ENSP00000453651.1:n.113+531T>C
ENST00000610490.4:c.146+531T>C	ENSP00000483762.1:n.146+531T>C
ENST00000622346.4:c.146+531T>C	ENSP00000479393.1:n.146+531T>C
NM_014862.3:c.146+531T>C	NP_055677.3:n.146+531T>C
NM_014862.4:c.146+531T>C MANE Select	NP_055677.3:n.146+531T>C