Canonical Allele Identifier: CA1141566137
Gene: LINC02775 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214088031T= , CM000663.2:g.214088031T= GRCh38
NC_000001.10:g.214261374T= , CM000663.1:g.214261374T= GRCh37
NC_000001.9:g.212327997T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15593A= XP_011508605.1:n.-188-15593A=
XR_922584.1:n.119-15593A=
XR_922584.2:n.261-15593A=