Canonical Allele Identifier: CA2629889034
Gene: ARNT2 HGNC NCBI

Linked Data

gnomAD v4: 15-80591548-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591548C>G , CM000677.2:g.80591548C>G GRCh38
NC_000015.9:g.80883889C>G , CM000677.1:g.80883889C>G GRCh37
NC_000015.8:g.78670944C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.1919-20C>G MANE Select ENSP00000307479.4:n.1919-20C>G
ENST00000303329.8:c.1919-20C>G ENSP00000307479.4:n.1919-20C>G
ENST00000527771.5:c.1886-20C>G ENSP00000453792.1:n.1886-20C>G
ENST00000533983.5:c.1886-20C>G ENSP00000453651.1:n.1886-20C>G
ENST00000610490.4:c.*217-20C>G ENSP00000483762.1:n.*217-20C>G
ENST00000622346.4:c.1919-20C>G ENSP00000479393.1:n.1919-20C>G
NM_014862.3:c.1919-20C>G NP_055677.3:n.1919-20C>G
NM_014862.4:c.1919-20C>G MANE Select NP_055677.3:n.1919-20C>G
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