Canonical Allele Identifier: CA2063275111
Gene: LINC02356 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399047C= , CM000674.2:g.111399047C= GRCh38
NC_000012.11:g.111836851C= , CM000674.1:g.111836851C= GRCh37
NC_000012.10:g.110321234C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2174C=