Canonical Allele Identifier: CA2165707045
Community Standard Title: NC_000015.10:g.26472746G=
Gene: LINC02248 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.26472746G= , CM000677.2:g.26472746G= GRCh38
NC_000015.9:g.26717893G= , CM000677.1:g.26717893G= GRCh37
NC_000015.8:g.24268986G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001751453.1:n.2717-16766G=
XR_001751456.1:n.419-1649C=
XR_001751457.1:n.419-1649C=
XR_001751458.1:n.419-1649C=
XR_001751459.1:n.419-1649C=
XR_932009.1:n.186-1649C=
XR_932010.1:n.186-1649C=