Canonical Allele Identifier: CA1427113061
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1722610140

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812771A>G , CM000665.2:g.186812771A>G GRCh38
NC_000003.11:g.186530560A>G , CM000665.1:g.186530560A>G GRCh37
NC_000003.10:g.188013254A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-623T>C