Canonical Allele Identifier: CA2486143541
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1571867447

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087913A>C , CM000663.2:g.214087913A>C GRCh38
NC_000001.10:g.214261256A>C , CM000663.1:g.214261256A>C GRCh37
NC_000001.9:g.212327879A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15475T>G XP_011508605.1:n.-188-15475T>G
XR_922584.1:n.119-15475T>G
XR_922584.2:n.261-15475T>G