Canonical Allele Identifier: CA1381162952
Gene: LINC02070 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495342G= , CM000665.2:g.86495342G= GRCh38
NC_000003.11:g.86544492G= , CM000665.1:g.86544492G= GRCh37
NC_000003.10:g.86627182G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-449G=
NR_135563.1:n.116-449G=