Canonical Allele Identifier: CA2486143473
Gene: LINC02775 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087723_214087724delinsCA , CM000663.2:g.214087723_214087724delinsCA GRCh38
NC_000001.10:g.214261066_214261067delinsCA , CM000663.1:g.214261066_214261067delinsCA GRCh37
NC_000001.9:g.212327689_212327690delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15286_-188-15285delinsTG XP_011508605.1:n.-188-15286_-188-15285delinsTG
XR_922584.1:n.119-15286_119-15285delinsTG
XR_922584.2:n.261-15286_261-15285delinsTG