Canonical Allele Identifier: CA903927133
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1382244258

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812676C>G , CM000665.2:g.186812676C>G GRCh38
NC_000003.11:g.186530465C>G , CM000665.1:g.186530465C>G GRCh37
NC_000003.10:g.188013159C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-528G>C