Canonical Allele Identifier: CA276296218

Gene: LINC02254 LINC02253

Linked Data

• dbSNP Id: rs748689198
• MyVariant Identifiers: chr15:g.97939170A>T (hg19) ; chr15:g.97395940A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.97395940A>T , CM000677.2:g.97395940A>T	GRCh38
NC_000015.9:g.97939170A>T , CM000677.1:g.97939170A>T	GRCh37
NC_000015.8:g.95740174A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120324.1:n.755+1717T>A (LINC02254)
XR_001751693.1:n.305-15252A>T (LINC02253)
XR_001751694.1:n.305-15252A>T (LINC02253)
XR_001751695.1:n.305-15252A>T (LINC02253)