Canonical Allele Identifier: CA2190458010

Gene: ARNT2

Linked Data

• dbSNP Id: rs1896392013

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80451615G>T , CM000677.2:g.80451615G>T	GRCh38
NC_000015.9:g.80743956G>T , CM000677.1:g.80743956G>T	GRCh37
NC_000015.8:g.78531011G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.146+621G>T MANE Select	ENSP00000307479.4:n.146+621G>T
ENST00000303329.8:c.146+621G>T	ENSP00000307479.4:n.146+621G>T
ENST00000525103.1:c.-57+10237G>T	ENSP00000452961.1:n.-57+10237G>T
ENST00000527771.5:c.113+621G>T	ENSP00000453792.1:n.113+621G>T
ENST00000529181.1:n.312+621G>T
ENST00000533983.5:c.113+621G>T	ENSP00000453651.1:n.113+621G>T
ENST00000610490.4:c.146+621G>T	ENSP00000483762.1:n.146+621G>T
ENST00000622346.4:c.146+621G>T	ENSP00000479393.1:n.146+621G>T
NM_014862.3:c.146+621G>T	NP_055677.3:n.146+621G>T
NM_014862.4:c.146+621G>T MANE Select	NP_055677.3:n.146+621G>T