Canonical Allele Identifier: CA274047418

Gene: ARNT2

Linked Data

• dbSNP Id: rs759350021
• gnomAD v3: 15-80591970-C-T
• gnomAD v4: 15-80591970-C-T
• MyVariant Identifiers: chr15:g.80884311C>T (hg19) ; chr15:g.80591970C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80591970C>T , CM000677.2:g.80591970C>T	GRCh38
NC_000015.9:g.80884311C>T , CM000677.1:g.80884311C>T	GRCh37
NC_000015.8:g.78671366C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.2055+266C>T MANE Select	ENSP00000307479.4:n.2055+266C>T
ENST00000303329.8:c.2055+266C>T	ENSP00000307479.4:n.2055+266C>T
ENST00000527771.5:c.2022+266C>T	ENSP00000453792.1:n.2022+266C>T
ENST00000533983.5:c.2022+266C>T	ENSP00000453651.1:n.2022+266C>T
ENST00000610490.4:c.*353+266C>T	ENSP00000483762.1:n.*353+266C>T
ENST00000622346.4:c.2055+266C>T	ENSP00000479393.1:n.2055+266C>T
NM_014862.3:c.2055+266C>T	NP_055677.3:n.2055+266C>T
NM_014862.4:c.2055+266C>T MANE Select	NP_055677.3:n.2055+266C>T