Canonical Allele Identifier: CA2486143486
Gene: LINC02775 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087757_214087758delinsTG , CM000663.2:g.214087757_214087758delinsTG GRCh38
NC_000001.10:g.214261100_214261101delinsTG , CM000663.1:g.214261100_214261101delinsTG GRCh37
NC_000001.9:g.212327723_212327724delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15320_-188-15319delinsCA XP_011508605.1:n.-188-15320_-188-15319delinsCA
XR_922584.1:n.119-15320_119-15319delinsCA
XR_922584.2:n.261-15320_261-15319delinsCA