Canonical Allele Identifier: CA911526718
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1394105043

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495209_86495212del , CM000665.2:g.86495209_86495212del GRCh38
NC_000003.11:g.86544359_86544362del , CM000665.1:g.86544359_86544362del GRCh37
NC_000003.10:g.86627049_86627052del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-582_116-579del
NR_135563.1:n.116-582_116-579del