Canonical Allele Identifier: CA2192802141
Gene: LINC02883 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756997C= , CM000677.2:g.85756997C= GRCh38
NC_000015.9:g.86300228C= , CM000677.1:g.86300228C= GRCh37
NC_000015.8:g.84101232C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120366.1:n.419+887G=