Canonical Allele Identifier: CA1057439559
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1722609792

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812715C>T , CM000665.2:g.186812715C>T GRCh38
NC_000003.11:g.186530504C>T , CM000665.1:g.186530504C>T GRCh37
NC_000003.10:g.188013198C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-567G>A