Canonical Allele Identifier: CA619996148
Gene: NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1342474535
gnomAD v2: 15-96830593-A-G
gnomAD v3: 15-96287364-A-G
gnomAD v4: 15-96287364-A-G
MyVariant Identifiers: chr15:g.96830593A>G (hg19) chr15:g.96287364A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96287364A>G , CM000677.2:g.96287364A>G GRCh38
NC_000015.9:g.96830593A>G , CM000677.1:g.96830593A>G GRCh37
NC_000015.8:g.94631597A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_102743.1:n.409+1300T>C
NR_125738.1:n.317+3266T>C
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