Canonical Allele Identifier: CA393624783
Gene: ARNT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.80883954A>C (hg19) chr15:g.80591613A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591613A>C , CM000677.2:g.80591613A>C GRCh38
NC_000015.9:g.80883954A>C , CM000677.1:g.80883954A>C GRCh37
NC_000015.8:g.78671009A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.1964A>C MANE Select ENSP00000307479.4:p.Glu655Ala
ENST00000303329.8:c.1964A>C ENSP00000307479.4:p.Glu655Ala
ENST00000527771.5:c.1931A>C ENSP00000453792.1:p.Glu644Ala
ENST00000533983.5:c.1931A>C ENSP00000453651.1:p.Glu644Ala
ENST00000610490.4:c.*262A>C ENSP00000483762.1:n.*262A>C
ENST00000622346.4:c.1964A>C ENSP00000479393.1:p.Glu655Ala
NM_014862.3:c.1964A>C NP_055677.3:p.Glu655Ala
NM_014862.4:c.1964A>C MANE Select NP_055677.3:p.Glu655Ala
Search 100 bp 5'
Search 100 bp 3'