Canonical Allele Identifier: CA393625462
Gene: ARNT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.80884041T>A (hg19) chr15:g.80591700T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591700T>A , CM000677.2:g.80591700T>A GRCh38
NC_000015.9:g.80884041T>A , CM000677.1:g.80884041T>A GRCh37
NC_000015.8:g.78671096T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.2051T>A MANE Select ENSP00000307479.4:p.Phe684Tyr
ENST00000303329.8:c.2051T>A ENSP00000307479.4:p.Phe684Tyr
ENST00000527771.5:c.2018T>A ENSP00000453792.1:p.Phe673Tyr
ENST00000533983.5:c.2018T>A ENSP00000453651.1:p.Phe673Tyr
ENST00000610490.4:c.*349T>A ENSP00000483762.1:n.*349T>A
ENST00000622346.4:c.2051T>A ENSP00000479393.1:p.Phe684Tyr
NM_014862.3:c.2051T>A NP_055677.3:p.Phe684Tyr
NM_014862.4:c.2051T>A MANE Select NP_055677.3:p.Phe684Tyr
Search 100 bp 5'
Search 100 bp 3'