Canonical Allele Identifier: CA2486143603
Gene: LINC02775 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214088061_214088062delinsCA , CM000663.2:g.214088061_214088062delinsCA GRCh38
NC_000001.10:g.214261404_214261405delinsCA , CM000663.1:g.214261404_214261405delinsCA GRCh37
NC_000001.9:g.212328027_212328028delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15624_-188-15623delinsTG XP_011508605.1:n.-188-15624_-188-15623delinsTG
XR_922584.1:n.119-15624_119-15623delinsTG
XR_922584.2:n.261-15624_261-15623delinsTG