Canonical Allele Identifier: CA911527330
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs71128153

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495301_86495306dup , CM000665.2:g.86495301_86495306dup GRCh38
NC_000003.11:g.86544451_86544456dup , CM000665.1:g.86544451_86544456dup GRCh37
NC_000003.10:g.86627141_86627146dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-490_116-485dup
NR_135563.1:n.116-490_116-485dup