Canonical Allele Identifier: CA7692223
Gene: ARNT2 HGNC NCBI

Linked Data

dbSNP Id: rs374287534
ExAC: 15:80883897 C / G
MyVariant Identifiers: chr15:g.80883897C>G (hg19) chr15:g.80591556C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591556C>G , CM000677.2:g.80591556C>G GRCh38
NC_000015.9:g.80883897C>G , CM000677.1:g.80883897C>G GRCh37
NC_000015.8:g.78670952C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.1919-12C>G MANE Select ENSP00000307479.4:n.1919-12C>G
ENST00000303329.8:c.1919-12C>G ENSP00000307479.4:n.1919-12C>G
ENST00000527771.5:c.1886-12C>G ENSP00000453792.1:n.1886-12C>G
ENST00000533983.5:c.1886-12C>G ENSP00000453651.1:n.1886-12C>G
ENST00000610490.4:c.*217-12C>G ENSP00000483762.1:n.*217-12C>G
ENST00000622346.4:c.1919-12C>G ENSP00000479393.1:n.1919-12C>G
NM_014862.3:c.1919-12C>G NP_055677.3:n.1919-12C>G
NM_014862.4:c.1919-12C>G MANE Select NP_055677.3:n.1919-12C>G
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