Canonical Allele Identifier: CA2486143513
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1665555881

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087846_214087862del , CM000663.2:g.214087846_214087862del GRCh38
NC_000001.10:g.214261189_214261205del , CM000663.1:g.214261189_214261205del GRCh37
NC_000001.9:g.212327812_212327828del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15422_-188-15406del XP_011508605.1:n.-188-15422_-188-15406del
XR_922584.1:n.119-15422_119-15406del
XR_922584.2:n.261-15422_261-15406del