Canonical Allele Identifier: CA2192802000
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs2089540178

Genomic Alleles

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

Transcript Alleles

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