Canonical Allele Identifier: CA2486143494
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1665555462

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087769A>G , CM000663.2:g.214087769A>G GRCh38
NC_000001.10:g.214261112A>G , CM000663.1:g.214261112A>G GRCh37
NC_000001.9:g.212327735A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15331T>C XP_011508605.1:n.-188-15331T>C
XR_922584.1:n.119-15331T>C
XR_922584.2:n.261-15331T>C