Canonical Allele Identifier: CA2192802028
Gene: LINC02883 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756936A= , CM000677.2:g.85756936A= GRCh38
NC_000015.9:g.86300167A= , CM000677.1:g.86300167A= GRCh37
NC_000015.8:g.84101171A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.419+948T=