Canonical Allele Identifier: CA2486143591
Gene: LINC02775 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214088028C= , CM000663.2:g.214088028C= GRCh38
NC_000001.10:g.214261371C= , CM000663.1:g.214261371C= GRCh37
NC_000001.9:g.212327994C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011510303.1:c.-188-15590G= XP_011508605.1:n.-188-15590G=
XR_922584.1:n.119-15590G=
XR_922584.2:n.261-15590G=