Canonical Allele Identifier: CA916400714
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1558205861

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087758del , CM000663.2:g.214087758del GRCh38
NC_000001.10:g.214261101del , CM000663.1:g.214261101del GRCh37
NC_000001.9:g.212327724del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15320del XP_011508605.1:n.-188-15320del
XR_922584.1:n.119-15320del
XR_922584.2:n.261-15320del