Canonical Allele Identifier: CA2731328679
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs2089540201

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756925A>G , CM000677.2:g.85756925A>G GRCh38
NC_000015.9:g.86300156A>G , CM000677.1:g.86300156A>G GRCh37
NC_000015.8:g.84101160A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.419+959T>C