Canonical Allele Identifier: CA1427113072
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs9857610

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-628C>G