Canonical Allele Identifier: CA646403935
Gene: LINC02775 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214088022dup , CM000663.2:g.214088022dup GRCh38
NC_000001.10:g.214261365dup , CM000663.1:g.214261365dup GRCh37
NC_000001.9:g.212327988dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15579dup XP_011508605.1:n.-188-15579dup
XR_922584.1:n.119-15579dup
XR_922584.2:n.261-15579dup