Canonical Allele Identifier: CA2486143529
Gene: LINC02775 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087893A= , CM000663.2:g.214087893A= GRCh38
NC_000001.10:g.214261236A= , CM000663.1:g.214261236A= GRCh37
NC_000001.9:g.212327859A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15455T= XP_011508605.1:n.-188-15455T=
XR_922584.1:n.119-15455T=
XR_922584.2:n.261-15455T=