Canonical Allele Identifier: CA1143939592
Gene: LINC02775 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087946A= , CM000663.2:g.214087946A= GRCh38
NC_000001.10:g.214261289A= , CM000663.1:g.214261289A= GRCh37
NC_000001.9:g.212327912A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15508T= XP_011508605.1:n.-188-15508T=
XR_922584.1:n.119-15508T=
XR_922584.2:n.261-15508T=