Canonical Allele Identifier: CA1427112932
Gene: LINC02043 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812658A= , CM000665.2:g.186812658A= GRCh38
NC_000003.11:g.186530447A= , CM000665.1:g.186530447A= GRCh37
NC_000003.10:g.188013141A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-510T=