Canonical Allele Identifier: CA2192802238
Gene: LINC02883 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85757036A= , CM000677.2:g.85757036A= GRCh38
NC_000015.9:g.86300267A= , CM000677.1:g.86300267A= GRCh37
NC_000015.8:g.84101271A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.419+848T=