Canonical Allele Identifier: CA1050454532
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1704111452

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495347del , CM000665.2:g.86495347del GRCh38
NC_000003.11:g.86544497del , CM000665.1:g.86544497del GRCh37
NC_000003.10:g.86627187del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-444del
NR_135563.1:n.116-444del