Canonical Allele Identifier: CA393625485
Gene: ARNT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591703A>T , CM000677.2:g.80591703A>T GRCh38
NC_000015.9:g.80884044A>T , CM000677.1:g.80884044A>T GRCh37
NC_000015.8:g.78671099A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.2054A>T MANE Select ENSP00000307479.4:p.Gln685Leu
ENST00000303329.8:c.2054A>T ENSP00000307479.4:p.Gln685Leu
ENST00000527771.5:c.2021A>T ENSP00000453792.1:p.Gln674Leu
ENST00000533983.5:c.2021A>T ENSP00000453651.1:p.Gln674Leu
ENST00000610490.4:c.*352A>T ENSP00000483762.1:n.*352A>T
ENST00000622346.4:c.2054A>T ENSP00000479393.1:p.Gln685Leu
NM_014862.3:c.2054A>T NP_055677.3:p.Gln685Leu
NM_014862.4:c.2054A>T MANE Select NP_055677.3:p.Gln685Leu