Canonical Allele Identifier: CA1427113096
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1722610576

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812803G>A , CM000665.2:g.186812803G>A GRCh38
NC_000003.11:g.186530592G>A , CM000665.1:g.186530592G>A GRCh37
NC_000003.10:g.188013286G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-655C>T