Canonical Allele Identifier: CA276166844
Gene: NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs904451293
gnomAD v3: 15-96301538-G-A
gnomAD v4: 15-96301538-G-A
MyVariant Identifiers: chr15:g.96844767G>A (hg19) chr15:g.96301538G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96301538G>A , CM000677.2:g.96301538G>A GRCh38
NC_000015.9:g.96844767G>A , CM000677.1:g.96844767G>A GRCh37
NC_000015.8:g.94645771G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_102743.1:n.164-10755C>T
NR_102744.1:n.164-10755C>T
NR_125738.1:n.164-10755C>T
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