Canonical Allele Identifier: CA7692227
Gene: ARNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2172006
ClinVar RCV Id: RCV003090443
dbSNP Id: rs201571391
ExAC: 15:80883928 C / T
gnomAD v2: 15-80883928-C-T
gnomAD v3: 15-80591587-C-T
gnomAD v4: 15-80591587-C-T
MyVariant Identifiers: chr15:g.80883928C>T (hg19) chr15:g.80591587C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591587C>T , CM000677.2:g.80591587C>T GRCh38
NC_000015.9:g.80883928C>T , CM000677.1:g.80883928C>T GRCh37
NC_000015.8:g.78670983C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.1938C>T MANE Select ENSP00000307479.4:p.Ser646=
ENST00000303329.8:c.1938C>T ENSP00000307479.4:p.Ser646=
ENST00000527771.5:c.1905C>T ENSP00000453792.1:p.Ser635=
ENST00000533983.5:c.1905C>T ENSP00000453651.1:p.Ser635=
ENST00000610490.4:c.*236C>T ENSP00000483762.1:n.*236C>T
ENST00000622346.4:c.1938C>T ENSP00000479393.1:p.Ser646=
NM_014862.3:c.1938C>T NP_055677.3:p.Ser646=
NM_014862.4:c.1938C>T MANE Select NP_055677.3:p.Ser646=
Search 100 bp 5'
Search 100 bp 3'