Canonical Allele Identifier: CA491688625

Gene: ARNT2

Linked Data

• dbSNP Id: rs1893280622
• gnomAD v4: 15-80591578-A-G
• MyVariant Identifiers: chr15:g.80883919A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80591578A>G , CM000677.2:g.80591578A>G	GRCh38
NC_000015.9:g.80883919A>G , CM000677.1:g.80883919A>G	GRCh37
NC_000015.8:g.78670974A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.1929A>G MANE Select	ENSP00000307479.4:p.Gly643=
ENST00000303329.8:c.1929A>G	ENSP00000307479.4:p.Gly643=
ENST00000527771.5:c.1896A>G	ENSP00000453792.1:p.Gly632=
ENST00000533983.5:c.1896A>G	ENSP00000453651.1:p.Gly632=
ENST00000610490.4:c.*227A>G	ENSP00000483762.1:n.*227A>G
ENST00000622346.4:c.1929A>G	ENSP00000479393.1:p.Gly643=
NM_014862.3:c.1929A>G	NP_055677.3:p.Gly643=
NM_014862.4:c.1929A>G MANE Select	NP_055677.3:p.Gly643=