Canonical Allele Identifier: CA1381162993
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1704111789

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495394_86495397del , CM000665.2:g.86495394_86495397del GRCh38
NC_000003.11:g.86544544_86544547del , CM000665.1:g.86544544_86544547del GRCh37
NC_000003.10:g.86627234_86627237del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-397_116-394del
NR_135563.1:n.116-397_116-394del