Canonical Allele Identifier: CA89646388
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs114161573

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812636G>A , CM000665.2:g.186812636G>A GRCh38
NC_000003.11:g.186530425G>A , CM000665.1:g.186530425G>A GRCh37
NC_000003.10:g.188013119G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-488C>T