Canonical Allele Identifier: CA1057439555
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1722609048

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812654T>C , CM000665.2:g.186812654T>C GRCh38
NC_000003.11:g.186530443T>C , CM000665.1:g.186530443T>C GRCh37
NC_000003.10:g.188013137T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-506A>G