Canonical Allele Identifier: CA2198524677
Gene: LINC02254 HGNC NCBI
LINC02253 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97396034T= , CM000677.2:g.97396034T= GRCh38
NC_000015.9:g.97939264T= , CM000677.1:g.97939264T= GRCh37
NC_000015.8:g.95740268T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120324.1:n.755+1623A= (LINC02254)
XR_001751693.1:n.305-15158T= (LINC02253)
XR_001751694.1:n.305-15158T= (LINC02253)
XR_001751695.1:n.305-15158T= (LINC02253)