Canonical Allele Identifier: CA2581238625
Gene: LINC02254 HGNC NCBI
LINC02253 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97395919A>C , CM000677.2:g.97395919A>C GRCh38
NC_000015.9:g.97939149A>C , CM000677.1:g.97939149A>C GRCh37
NC_000015.8:g.95740153A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120324.1:n.755+1738T>G (LINC02254)
XR_001751693.1:n.305-15273A>C (LINC02253)
XR_001751694.1:n.305-15273A>C (LINC02253)
XR_001751695.1:n.305-15273A>C (LINC02253)