Canonical Allele Identifier: CA2486143449
Gene: LINC02775 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087668_214087672delinsCTTTA , CM000663.2:g.214087668_214087672delinsCTTTA GRCh38
NC_000001.10:g.214261011_214261015delinsCTTTA , CM000663.1:g.214261011_214261015delinsCTTTA GRCh37
NC_000001.9:g.212327634_212327638delinsCTTTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15234_-188-15230delinsTAAAG XP_011508605.1:n.-188-15234_-188-15230delinsTAAAG
XR_922584.1:n.119-15234_119-15230delinsTAAAG
XR_922584.2:n.261-15234_261-15230delinsTAAAG