Canonical Allele Identifier: CA2505222116
Gene: LINC02883 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756935A>G , CM000677.2:g.85756935A>G GRCh38
NC_000015.9:g.86300166A>G , CM000677.1:g.86300166A>G GRCh37
NC_000015.8:g.84101170A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.419+949T>C