Canonical Allele Identifier: CA2165708981
Community Standard Title: NC_000015.10:g.26475396A=
Gene: LINC02248 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.26475396A= , CM000677.2:g.26475396A= GRCh38
NC_000015.9:g.26720543A= , CM000677.1:g.26720543A= GRCh37
NC_000015.8:g.24271636A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001751453.1:n.2717-14116A=
XR_001751456.1:n.418+2325T=
XR_001751457.1:n.418+2325T=
XR_001751458.1:n.418+2325T=
XR_001751459.1:n.418+2325T=
XR_932009.1:n.185+2325T=
XR_932010.1:n.185+2325T=