Canonical Allele Identifier: CA393624774
Gene: ARNT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.80883950T>A (hg19) chr15:g.80591609T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591609T>A , CM000677.2:g.80591609T>A GRCh38
NC_000015.9:g.80883950T>A , CM000677.1:g.80883950T>A GRCh37
NC_000015.8:g.78671005T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.1960T>A MANE Select ENSP00000307479.4:p.Ser654Thr
ENST00000303329.8:c.1960T>A ENSP00000307479.4:p.Ser654Thr
ENST00000527771.5:c.1927T>A ENSP00000453792.1:p.Ser643Thr
ENST00000533983.5:c.1927T>A ENSP00000453651.1:p.Ser643Thr
ENST00000610490.4:c.*258T>A ENSP00000483762.1:n.*258T>A
ENST00000622346.4:c.1960T>A ENSP00000479393.1:p.Ser654Thr
NM_014862.3:c.1960T>A NP_055677.3:p.Ser654Thr
NM_014862.4:c.1960T>A MANE Select NP_055677.3:p.Ser654Thr
Search 100 bp 5'
Search 100 bp 3'