Canonical Allele Identifier: CA913385326
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1558205858

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087752T>C , CM000663.2:g.214087752T>C GRCh38
NC_000001.10:g.214261095T>C , CM000663.1:g.214261095T>C GRCh37
NC_000001.9:g.212327718T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15314A>G XP_011508605.1:n.-188-15314A>G
XR_922584.1:n.119-15314A>G
XR_922584.2:n.261-15314A>G