Canonical Allele Identifier: CA2190489794
Gene: ARNT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591737A= , CM000677.2:g.80591737A= GRCh38
NC_000015.9:g.80884078A= , CM000677.1:g.80884078A= GRCh37
NC_000015.8:g.78671133A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.2055+33A= MANE Select ENSP00000307479.4:n.2055+33A=
ENST00000303329.8:c.2055+33A= ENSP00000307479.4:n.2055+33A=
ENST00000527771.5:c.2022+33A= ENSP00000453792.1:n.2022+33A=
ENST00000533983.5:c.2022+33A= ENSP00000453651.1:n.2022+33A=
ENST00000610490.4:c.*353+33A= ENSP00000483762.1:n.*353+33A=
ENST00000622346.4:c.2055+33A= ENSP00000479393.1:n.2055+33A=
NM_014862.3:c.2055+33A= NP_055677.3:n.2055+33A=
NM_014862.4:c.2055+33A= MANE Select NP_055677.3:n.2055+33A=
Search 100 bp 5'
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