Canonical Allele Identifier: CA1050454449
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1704111071

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495313_86495315del , CM000665.2:g.86495313_86495315del GRCh38
NC_000003.11:g.86544463_86544465del , CM000665.1:g.86544463_86544465del GRCh37
NC_000003.10:g.86627153_86627155del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-478_116-476del
NR_135563.1:n.116-478_116-476del