Canonical Allele Identifier: CA1381162349
Gene: LINC02070 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495238T= , CM000665.2:g.86495238T= GRCh38
NC_000003.11:g.86544388T= , CM000665.1:g.86544388T= GRCh37
NC_000003.10:g.86627078T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245082.1:n.116-553T=
NR_135563.1:n.116-553T=