Canonical Allele Identifier: CA89646496
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs916666020

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812786A>G , CM000665.2:g.186812786A>G GRCh38
NC_000003.11:g.186530575A>G , CM000665.1:g.186530575A>G GRCh37
NC_000003.10:g.188013269A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-638T>C