Canonical Allele Identifier: CA2486143452
Gene: LINC02775 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087673_214087678delinsTTTATA , CM000663.2:g.214087673_214087678delinsTTTATA GRCh38
NC_000001.10:g.214261016_214261021delinsTTTATA , CM000663.1:g.214261016_214261021delinsTTTATA GRCh37
NC_000001.9:g.212327639_212327644delinsTTTATA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15240_-188-15235delinsTATAAA XP_011508605.1:n.-188-15240_-188-15235delinsTATAAA
XR_922584.1:n.119-15240_119-15235delinsTATAAA
XR_922584.2:n.261-15240_261-15235delinsTATAAA