Canonical Allele Identifier: CA7692244
Gene: ARNT2 HGNC NCBI

Linked Data

dbSNP Id: rs140703832
ExAC: 15:80884024 C / G
gnomAD v2: 15-80884024-C-G
gnomAD v4: 15-80591683-C-G
MyVariant Identifiers: chr15:g.80884024C>G (hg19) chr15:g.80591683C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591683C>G , CM000677.2:g.80591683C>G GRCh38
NC_000015.9:g.80884024C>G , CM000677.1:g.80884024C>G GRCh37
NC_000015.8:g.78671079C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.2034C>G MANE Select ENSP00000307479.4:p.Pro678=
ENST00000303329.8:c.2034C>G ENSP00000307479.4:p.Pro678=
ENST00000527771.5:c.2001C>G ENSP00000453792.1:p.Pro667=
ENST00000533983.5:c.2001C>G ENSP00000453651.1:p.Pro667=
ENST00000610490.4:c.*332C>G ENSP00000483762.1:n.*332C>G
ENST00000622346.4:c.2034C>G ENSP00000479393.1:p.Pro678=
NM_014862.3:c.2034C>G NP_055677.3:p.Pro678=
NM_014862.4:c.2034C>G MANE Select NP_055677.3:p.Pro678=
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