Canonical Allele Identifier: CA2192802032
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs2089540261

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756945C>G , CM000677.2:g.85756945C>G GRCh38
NC_000015.9:g.86300176C>G , CM000677.1:g.86300176C>G GRCh37
NC_000015.8:g.84101180C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.419+939G>C