Canonical Allele Identifier: CA1427112958
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1722609382

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812689C>A , CM000665.2:g.186812689C>A GRCh38
NC_000003.11:g.186530478C>A , CM000665.1:g.186530478C>A GRCh37
NC_000003.10:g.188013172C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-541G>T