Canonical Allele Identifier: CA619996151
Gene: NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1337931728
gnomAD v2: 15-96830645-C-G
gnomAD v3: 15-96287416-C-G
gnomAD v4: 15-96287416-C-G
MyVariant Identifiers: chr15:g.96830645C>G (hg19) chr15:g.96287416C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96287416C>G , CM000677.2:g.96287416C>G GRCh38
NC_000015.9:g.96830645C>G , CM000677.1:g.96830645C>G GRCh37
NC_000015.8:g.94631649C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_102743.1:n.409+1248G>C
NR_125738.1:n.317+3214G>C
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