Canonical Allele Identifier: CA2192801998
Gene: LINC02883 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756923C= , CM000677.2:g.85756923C= GRCh38
NC_000015.9:g.86300154C= , CM000677.1:g.86300154C= GRCh37
NC_000015.8:g.84101158C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.419+961G=