Canonical Allele Identifier: CA89646487
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs9857610

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812776G>T , CM000665.2:g.186812776G>T GRCh38
NC_000003.11:g.186530565G>T , CM000665.1:g.186530565G>T GRCh37
NC_000003.10:g.188013259G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-628C>A