Canonical Allele Identifier: CA276165224
Gene: NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs755890079
gnomAD v4: 15-96287090-T-C
MyVariant Identifiers: chr15:g.96830319T>C (hg19) chr15:g.96287090T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96287090T>C , CM000677.2:g.96287090T>C GRCh38
NC_000015.9:g.96830319T>C , CM000677.1:g.96830319T>C GRCh37
NC_000015.8:g.94631323T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102743.1:n.409+1574A>G
NR_125738.1:n.317+3540A>G
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