Canonical Allele Identifier: CA1427112965
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1722609466

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812694G>A , CM000665.2:g.186812694G>A GRCh38
NC_000003.11:g.186530483G>A , CM000665.1:g.186530483G>A GRCh37
NC_000003.10:g.188013177G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-546C>T