Canonical Allele Identifier: CA393625137
Gene: ARNT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.80883985T>G (hg19) chr15:g.80591644T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591644T>G , CM000677.2:g.80591644T>G GRCh38
NC_000015.9:g.80883985T>G , CM000677.1:g.80883985T>G GRCh37
NC_000015.8:g.78671040T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.1995T>G MANE Select ENSP00000307479.4:p.His665Gln
ENST00000303329.8:c.1995T>G ENSP00000307479.4:p.His665Gln
ENST00000527771.5:c.1962T>G ENSP00000453792.1:p.His654Gln
ENST00000533983.5:c.1962T>G ENSP00000453651.1:p.His654Gln
ENST00000610490.4:c.*293T>G ENSP00000483762.1:n.*293T>G
ENST00000622346.4:c.1995T>G ENSP00000479393.1:p.His665Gln
NM_014862.3:c.1995T>G NP_055677.3:p.His665Gln
NM_014862.4:c.1995T>G MANE Select NP_055677.3:p.His665Gln
Search 100 bp 5'
Search 100 bp 3'