Canonical Allele Identifier: CA973205596
Gene: LINC02254 HGNC NCBI
LINC02253 HGNC NCBI

Linked Data

dbSNP Id: rs1898054753
gnomAD v3: 15-97396072-G-A
gnomAD v4: 15-97396072-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97396072G>A , CM000677.2:g.97396072G>A GRCh38
NC_000015.9:g.97939302G>A , CM000677.1:g.97939302G>A GRCh37
NC_000015.8:g.95740306G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120324.1:n.755+1585C>T (LINC02254)
XR_001751693.1:n.305-15120G>A (LINC02253)
XR_001751694.1:n.305-15120G>A (LINC02253)
XR_001751695.1:n.305-15120G>A (LINC02253)
Search 100 bp 5'
Search 100 bp 3'