Canonical Allele Identifier: CA89646406
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs527965616

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812672C>T , CM000665.2:g.186812672C>T GRCh38
NC_000003.11:g.186530461C>T , CM000665.1:g.186530461C>T GRCh37
NC_000003.10:g.188013155C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-524G>A