Canonical Allele Identifier: CA2805377165
Gene: LINC02254 HGNC NCBI
LINC02253 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97396088C>T , CM000677.2:g.97396088C>T GRCh38
NC_000015.9:g.97939318C>T , CM000677.1:g.97939318C>T GRCh37
NC_000015.8:g.95740322C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120324.1:n.755+1569G>A (LINC02254)
XR_001751693.1:n.305-15104C>T (LINC02253)
XR_001751694.1:n.305-15104C>T (LINC02253)
XR_001751695.1:n.305-15104C>T (LINC02253)