Canonical Allele Identifier: CA1381162906
Gene: LINC02070 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-478G=
NR_135563.1:n.116-478G=