Canonical Allele Identifier: CA528919722
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1162283735

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087676A>G , CM000663.2:g.214087676A>G GRCh38
NC_000001.10:g.214261019A>G , CM000663.1:g.214261019A>G GRCh37
NC_000001.9:g.212327642A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15238T>C XP_011508605.1:n.-188-15238T>C
XR_922584.1:n.119-15238T>C
XR_922584.2:n.261-15238T>C