Canonical Allele Identifier: CA716126297
Gene: ARNT2 HGNC NCBI

Linked Data

dbSNP Id: rs1165450151
gnomAD v3: 15-80591955-A-T
gnomAD v4: 15-80591955-A-T
MyVariant Identifiers: chr15:g.80884296A>T (hg19) chr15:g.80591955A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591955A>T , CM000677.2:g.80591955A>T GRCh38
NC_000015.9:g.80884296A>T , CM000677.1:g.80884296A>T GRCh37
NC_000015.8:g.78671351A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.2055+251A>T MANE Select ENSP00000307479.4:n.2055+251A>T
ENST00000303329.8:c.2055+251A>T ENSP00000307479.4:n.2055+251A>T
ENST00000527771.5:c.2022+251A>T ENSP00000453792.1:n.2022+251A>T
ENST00000533983.5:c.2022+251A>T ENSP00000453651.1:n.2022+251A>T
ENST00000610490.4:c.*353+251A>T ENSP00000483762.1:n.*353+251A>T
ENST00000622346.4:c.2055+251A>T ENSP00000479393.1:n.2055+251A>T
NM_014862.3:c.2055+251A>T NP_055677.3:n.2055+251A>T
NM_014862.4:c.2055+251A>T MANE Select NP_055677.3:n.2055+251A>T
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