Canonical Allele Identifier: CA903927127
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1293003165

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812658A>T , CM000665.2:g.186812658A>T GRCh38
NC_000003.11:g.186530447A>T , CM000665.1:g.186530447A>T GRCh37
NC_000003.10:g.188013141A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-510T>A