Canonical Allele Identifier: CA89646467
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1018773350

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812730G>T , CM000665.2:g.186812730G>T GRCh38
NC_000003.11:g.186530519G>T , CM000665.1:g.186530519G>T GRCh37
NC_000003.10:g.188013213G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-582C>A