Canonical Allele Identifier: CA903927131
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1324282882

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812663T>C , CM000665.2:g.186812663T>C GRCh38
NC_000003.11:g.186530452T>C , CM000665.1:g.186530452T>C GRCh37
NC_000003.10:g.188013146T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-515A>G