Canonical Allele Identifier: CA916400715
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1571867494

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214088044_214088046del , CM000663.2:g.214088044_214088046del GRCh38
NC_000001.10:g.214261387_214261389del , CM000663.1:g.214261387_214261389del GRCh37
NC_000001.9:g.212328010_212328012del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15605_-188-15603del XP_011508605.1:n.-188-15605_-188-15603del
XR_922584.1:n.119-15605_119-15603del
XR_922584.2:n.261-15605_261-15603del