Canonical Allele Identifier: CA2731546184
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs2151802197

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756824A>G , CM000677.2:g.85756824A>G GRCh38
NC_000015.9:g.86300055A>G , CM000677.1:g.86300055A>G GRCh37
NC_000015.8:g.84101059A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.420-868T>C