Canonical Allele Identifier: CA1050454047
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1704109065

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495276_86495277insTTATATAT , CM000665.2:g.86495276_86495277insTTATATAT GRCh38
NC_000003.11:g.86544426_86544427insTTATATAT , CM000665.1:g.86544426_86544427insTTATATAT GRCh37
NC_000003.10:g.86627116_86627117insTTATATAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-515_116-514insTTATATAT
NR_135563.1:n.116-515_116-514insTTATATAT