Canonical Allele Identifier: CA2192801988
Gene: LINC02883 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756913T= , CM000677.2:g.85756913T= GRCh38
NC_000015.9:g.86300144T= , CM000677.1:g.86300144T= GRCh37
NC_000015.8:g.84101148T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120366.1:n.420-957A=