Canonical Allele Identifier: CA1057439569
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs897914370

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812740C>G , CM000665.2:g.186812740C>G GRCh38
NC_000003.11:g.186530529C>G , CM000665.1:g.186530529C>G GRCh37
NC_000003.10:g.188013223C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-592G>C