Canonical Allele Identifier: CA276165265
Gene: NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs577153362
gnomAD v2: 15-96830664-C-T
gnomAD v3: 15-96287435-C-T
gnomAD v4: 15-96287435-C-T
MyVariant Identifiers: chr15:g.96830664C>T (hg19) chr15:g.96287435C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96287435C>T , CM000677.2:g.96287435C>T GRCh38
NC_000015.9:g.96830664C>T , CM000677.1:g.96830664C>T GRCh37
NC_000015.8:g.94631668C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_102743.1:n.409+1229G>A
NR_125738.1:n.317+3195G>A
Search 100 bp 5'
Search 100 bp 3'