Canonical Allele Identifier: CA1427112939
Gene: LINC02043 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812672C= , CM000665.2:g.186812672C= GRCh38
NC_000003.11:g.186530461C= , CM000665.1:g.186530461C= GRCh37
NC_000003.10:g.188013155C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-524G=