Canonical Allele Identifier: CA1427112980
Gene: LINC02043 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812705T= , CM000665.2:g.186812705T= GRCh38
NC_000003.11:g.186530494T= , CM000665.1:g.186530494T= GRCh37
NC_000003.10:g.188013188T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-557A=