Canonical Allele Identifier: CA393625248
Gene: ARNT2 HGNC NCBI

Linked Data

dbSNP Id: rs1449107939

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591663C>G , CM000677.2:g.80591663C>G GRCh38
NC_000015.9:g.80884004C>G , CM000677.1:g.80884004C>G GRCh37
NC_000015.8:g.78671059C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.2014C>G MANE Select ENSP00000307479.4:p.Gln672Glu
ENST00000303329.8:c.2014C>G ENSP00000307479.4:p.Gln672Glu
ENST00000527771.5:c.1981C>G ENSP00000453792.1:p.Gln661Glu
ENST00000533983.5:c.1981C>G ENSP00000453651.1:p.Gln661Glu
ENST00000610490.4:c.*312C>G ENSP00000483762.1:n.*312C>G
ENST00000622346.4:c.2014C>G ENSP00000479393.1:p.Gln672Glu
NM_014862.3:c.2014C>G NP_055677.3:p.Gln672Glu
NM_014862.4:c.2014C>G MANE Select NP_055677.3:p.Gln672Glu