Canonical Allele Identifier: CA393625297
Gene: ARNT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591672C>A , CM000677.2:g.80591672C>A GRCh38
NC_000015.9:g.80884013C>A , CM000677.1:g.80884013C>A GRCh37
NC_000015.8:g.78671068C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.2023C>A MANE Select ENSP00000307479.4:p.His675Asn
ENST00000303329.8:c.2023C>A ENSP00000307479.4:p.His675Asn
ENST00000527771.5:c.1990C>A ENSP00000453792.1:p.His664Asn
ENST00000533983.5:c.1990C>A ENSP00000453651.1:p.His664Asn
ENST00000610490.4:c.*321C>A ENSP00000483762.1:n.*321C>A
ENST00000622346.4:c.2023C>A ENSP00000479393.1:p.His675Asn
NM_014862.3:c.2023C>A NP_055677.3:p.His675Asn
NM_014862.4:c.2023C>A MANE Select NP_055677.3:p.His675Asn