Canonical Allele Identifier: CA2606867637
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs2108477957

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812706del , CM000665.2:g.186812706del GRCh38
NC_000003.11:g.186530495del , CM000665.1:g.186530495del GRCh37
NC_000003.10:g.188013189del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-558del