Canonical Allele Identifier: CA717621042
Gene: LINC02254 HGNC NCBI
LINC02253 HGNC NCBI

Linked Data

dbSNP Id: rs1225320769
MyVariant Identifiers: chr15:g.97939305C>T (hg19) chr15:g.97396075C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97396075C>T , CM000677.2:g.97396075C>T GRCh38
NC_000015.9:g.97939305C>T , CM000677.1:g.97939305C>T GRCh37
NC_000015.8:g.95740309C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120324.1:n.755+1582G>A (LINC02254)
XR_001751693.1:n.305-15117C>T (LINC02253)
XR_001751694.1:n.305-15117C>T (LINC02253)
XR_001751695.1:n.305-15117C>T (LINC02253)
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