Canonical Allele Identifier: CA2349984594
Gene: LINC02871 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10869816G= , CM000682.2:g.10869816G= GRCh38
NC_000020.10:g.10850464G= , CM000682.1:g.10850464G= GRCh37
NC_000020.9:g.10798464G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937255.1:n.2829+2509G=