Canonical Allele Identifier: CA2486143467
Gene: LINC02775 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087712_214087713delinsTC , CM000663.2:g.214087712_214087713delinsTC GRCh38
NC_000001.10:g.214261055_214261056delinsTC , CM000663.1:g.214261055_214261056delinsTC GRCh37
NC_000001.9:g.212327678_212327679delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15275_-188-15274delinsGA XP_011508605.1:n.-188-15275_-188-15274delinsGA
XR_922584.1:n.119-15275_119-15274delinsGA
XR_922584.2:n.261-15275_261-15274delinsGA