Canonical Allele Identifier: CA2486143462
Gene: LINC02775 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087690_214087691delinsGA , CM000663.2:g.214087690_214087691delinsGA GRCh38
NC_000001.10:g.214261033_214261034delinsGA , CM000663.1:g.214261033_214261034delinsGA GRCh37
NC_000001.9:g.212327656_212327657delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15253_-188-15252delinsTC XP_011508605.1:n.-188-15253_-188-15252delinsTC
XR_922584.1:n.119-15253_119-15252delinsTC
XR_922584.2:n.261-15253_261-15252delinsTC