Canonical Allele Identifier: CA7692236
Gene: ARNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2305010
ClinVar RCV Id: RCV004149097
dbSNP Id: rs555361235
ExAC: 15:80883972 A / G
gnomAD v2: 15-80883972-A-G
gnomAD v3: 15-80591631-A-G
gnomAD v4: 15-80591631-A-G
MyVariant Identifiers: chr15:g.80883972A>G (hg19) chr15:g.80591631A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591631A>G , CM000677.2:g.80591631A>G GRCh38
NC_000015.9:g.80883972A>G , CM000677.1:g.80883972A>G GRCh37
NC_000015.8:g.78671027A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.1982A>G MANE Select ENSP00000307479.4:p.Gln661Arg
ENST00000303329.8:c.1982A>G ENSP00000307479.4:p.Gln661Arg
ENST00000527771.5:c.1949A>G ENSP00000453792.1:p.Gln650Arg
ENST00000533983.5:c.1949A>G ENSP00000453651.1:p.Gln650Arg
ENST00000610490.4:c.*280A>G ENSP00000483762.1:n.*280A>G
ENST00000622346.4:c.1982A>G ENSP00000479393.1:p.Gln661Arg
NM_014862.3:c.1982A>G NP_055677.3:p.Gln661Arg
NM_014862.4:c.1982A>G MANE Select NP_055677.3:p.Gln661Arg
Search 100 bp 5'
Search 100 bp 3'