Canonical Allele Identifier: CA2192802040
Gene: LINC02883 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756946C= , CM000677.2:g.85756946C= GRCh38
NC_000015.9:g.86300177C= , CM000677.1:g.86300177C= GRCh37
NC_000015.8:g.84101181C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.419+938G=