Canonical Allele Identifier: CA1427112764
Gene: LINC02043 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812519A= , CM000665.2:g.186812519A= GRCh38
NC_000003.11:g.186530308A= , CM000665.1:g.186530308A= GRCh37
NC_000003.10:g.188013002A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-371T=