Canonical Allele Identifier: CA89646483
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1028080599

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812774A>G , CM000665.2:g.186812774A>G GRCh38
NC_000003.11:g.186530563A>G , CM000665.1:g.186530563A>G GRCh37
NC_000003.10:g.188013257A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-626T>C