Canonical Allele Identifier: CA1057439520
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1722606526

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812512A>G , CM000665.2:g.186812512A>G GRCh38
NC_000003.11:g.186530301A>G , CM000665.1:g.186530301A>G GRCh37
NC_000003.10:g.188012995A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-364T>C