Canonical Allele Identifier: CA717519662
Gene: NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1449714457
gnomAD v3: 15-96287418-G-A
gnomAD v4: 15-96287418-G-A
MyVariant Identifiers: chr15:g.96830647G>A (hg19) chr15:g.96287418G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96287418G>A , CM000677.2:g.96287418G>A GRCh38
NC_000015.9:g.96830647G>A , CM000677.1:g.96830647G>A GRCh37
NC_000015.8:g.94631651G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_102743.1:n.409+1246C>T
NR_125738.1:n.317+3212C>T
Search 100 bp 5'
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