Canonical Allele Identifier: CA491688697
Gene: ARNT2 HGNC NCBI

Linked Data

dbSNP Id: rs77894979
gnomAD v4: 15-80591623-G-C
MyVariant Identifiers: chr15:g.80883964G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591623G>C , CM000677.2:g.80591623G>C GRCh38
NC_000015.9:g.80883964G>C , CM000677.1:g.80883964G>C GRCh37
NC_000015.8:g.78671019G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.1974G>C MANE Select ENSP00000307479.4:p.Ser658=
ENST00000303329.8:c.1974G>C ENSP00000307479.4:p.Ser658=
ENST00000527771.5:c.1941G>C ENSP00000453792.1:p.Ser647=
ENST00000533983.5:c.1941G>C ENSP00000453651.1:p.Ser647=
ENST00000610490.4:c.*272G>C ENSP00000483762.1:n.*272G>C
ENST00000622346.4:c.1974G>C ENSP00000479393.1:p.Ser658=
NM_014862.3:c.1974G>C NP_055677.3:p.Ser658=
NM_014862.4:c.1974G>C MANE Select NP_055677.3:p.Ser658=
Search 100 bp 5'
Search 100 bp 3'