Canonical Allele Identifier: CA37393420
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1039366517

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087929G>C , CM000663.2:g.214087929G>C GRCh38
NC_000001.10:g.214261272G>C , CM000663.1:g.214261272G>C GRCh37
NC_000001.9:g.212327895G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15491C>G XP_011508605.1:n.-188-15491C>G
XR_922584.1:n.119-15491C>G
XR_922584.2:n.261-15491C>G