Canonical Allele Identifier: CA1427112934
Gene: LINC02043 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812659C= , CM000665.2:g.186812659C= GRCh38
NC_000003.11:g.186530448C= , CM000665.1:g.186530448C= GRCh37
NC_000003.10:g.188013142C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-511G=