Canonical Allele Identifier: CA2805072193
Gene: LINC02883 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85757024G>T , CM000677.2:g.85757024G>T GRCh38
NC_000015.9:g.86300255G>T , CM000677.1:g.86300255G>T GRCh37
NC_000015.8:g.84101259G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.419+860C>A