Canonical Allele Identifier: CA619996149
Gene: NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1251093563
gnomAD v2: 15-96830643-C-A
gnomAD v3: 15-96287414-C-A
gnomAD v4: 15-96287414-C-A
MyVariant Identifiers: chr15:g.96830643C>A (hg19) chr15:g.96287414C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96287414C>A , CM000677.2:g.96287414C>A GRCh38
NC_000015.9:g.96830643C>A , CM000677.1:g.96830643C>A GRCh37
NC_000015.8:g.94631647C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_102743.1:n.409+1250G>T
NR_125738.1:n.317+3216G>T
Search 100 bp 5'
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