Canonical Allele Identifier: CA717519442
Gene: NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1426569146
gnomAD v3: 15-96287005-T-C
gnomAD v4: 15-96287005-T-C
MyVariant Identifiers: chr15:g.96830234T>C (hg19) chr15:g.96287005T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96287005T>C , CM000677.2:g.96287005T>C GRCh38
NC_000015.9:g.96830234T>C , CM000677.1:g.96830234T>C GRCh37
NC_000015.8:g.94631238T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102743.1:n.410-1546A>G
NR_125738.1:n.317+3625A>G
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