Canonical Allele Identifier: CA393624711
Gene: ARNT2 HGNC NCBI

Linked Data

gnomAD v4: 15-80591580-A-G
MyVariant Identifiers: chr15:g.80883921A>G (hg19) chr15:g.80591580A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591580A>G , CM000677.2:g.80591580A>G GRCh38
NC_000015.9:g.80883921A>G , CM000677.1:g.80883921A>G GRCh37
NC_000015.8:g.78670976A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.1931A>G MANE Select ENSP00000307479.4:p.Gln644Arg
ENST00000303329.8:c.1931A>G ENSP00000307479.4:p.Gln644Arg
ENST00000527771.5:c.1898A>G ENSP00000453792.1:p.Gln633Arg
ENST00000533983.5:c.1898A>G ENSP00000453651.1:p.Gln633Arg
ENST00000610490.4:c.*229A>G ENSP00000483762.1:n.*229A>G
ENST00000622346.4:c.1931A>G ENSP00000479393.1:p.Gln644Arg
NM_014862.3:c.1931A>G NP_055677.3:p.Gln644Arg
NM_014862.4:c.1931A>G MANE Select NP_055677.3:p.Gln644Arg
Search 100 bp 5'
Search 100 bp 3'