Canonical Allele Identifier: CA276165263
Gene: NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs150861714
gnomAD v2: 15-96830651-G-A
gnomAD v3: 15-96287422-G-A
gnomAD v4: 15-96287422-G-A
MyVariant Identifiers: chr15:g.96830651G>A (hg19) chr15:g.96287422G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96287422G>A , CM000677.2:g.96287422G>A GRCh38
NC_000015.9:g.96830651G>A , CM000677.1:g.96830651G>A GRCh37
NC_000015.8:g.94631655G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_102743.1:n.409+1242C>T
NR_125738.1:n.317+3208C>T
Search 100 bp 5'
Search 100 bp 3'