Canonical Allele Identifier: CA2192801984
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs2089540142

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756911G>A , CM000677.2:g.85756911G>A GRCh38
NC_000015.9:g.86300142G>A , CM000677.1:g.86300142G>A GRCh37
NC_000015.8:g.84101146G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.420-955C>T