Canonical Allele Identifier: CA619996136
Gene: NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1250385353
gnomAD v2: 15-96830372-C-T
gnomAD v3: 15-96287143-C-T
gnomAD v4: 15-96287143-C-T
MyVariant Identifiers: chr15:g.96830372C>T (hg19) chr15:g.96287143C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96287143C>T , CM000677.2:g.96287143C>T GRCh38
NC_000015.9:g.96830372C>T , CM000677.1:g.96830372C>T GRCh37
NC_000015.8:g.94631376C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_102743.1:n.409+1521G>A
NR_125738.1:n.317+3487G>A
Search 100 bp 5'
Search 100 bp 3'