Canonical Allele Identifier: CA1012083004
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1665555435

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087768A>C , CM000663.2:g.214087768A>C GRCh38
NC_000001.10:g.214261111A>C , CM000663.1:g.214261111A>C GRCh37
NC_000001.9:g.212327734A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15330T>G XP_011508605.1:n.-188-15330T>G
XR_922584.1:n.119-15330T>G
XR_922584.2:n.261-15330T>G