Canonical Allele Identifier: CA717519575
Gene: NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1297968834
MyVariant Identifiers: chr15:g.96830445C>T (hg19) chr15:g.96287216C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96287216C>T , CM000677.2:g.96287216C>T GRCh38
NC_000015.9:g.96830445C>T , CM000677.1:g.96830445C>T GRCh37
NC_000015.8:g.94631449C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_102743.1:n.409+1448G>A
NR_125738.1:n.317+3414G>A
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