Canonical Allele Identifier: CA276166842
Gene: NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs150734475
gnomAD v2: 15-96844733-G-T
gnomAD v3: 15-96301504-G-T
gnomAD v4: 15-96301504-G-T
MyVariant Identifiers: chr15:g.96844733G>T (hg19) chr15:g.96301504G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96301504G>T , CM000677.2:g.96301504G>T GRCh38
NC_000015.9:g.96844733G>T , CM000677.1:g.96844733G>T GRCh37
NC_000015.8:g.94645737G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102743.1:n.164-10721C>A
NR_102744.1:n.164-10721C>A
NR_125738.1:n.164-10721C>A
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