Canonical Allele Identifier: CA973205530
Gene: LINC02254 HGNC NCBI
LINC02253 HGNC NCBI

Linked Data

dbSNP Id: rs1898051472

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97395921_97395922del , CM000677.2:g.97395921_97395922del GRCh38
NC_000015.9:g.97939151_97939152del , CM000677.1:g.97939151_97939152del GRCh37
NC_000015.8:g.95740155_95740156del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120324.1:n.755+1739_755+1740del (LINC02254)
XR_001751693.1:n.305-15271_305-15270del (LINC02253)
XR_001751694.1:n.305-15271_305-15270del (LINC02253)
XR_001751695.1:n.305-15271_305-15270del (LINC02253)