Canonical Allele Identifier: CA2486143470

Gene: LINC02775

Linked Data

• dbSNP Id: rs1665554988

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214087715C>G , CM000663.2:g.214087715C>G	GRCh38
NC_000001.10:g.214261058C>G , CM000663.1:g.214261058C>G	GRCh37
NC_000001.9:g.212327681C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510303.1:c.-188-15277G>C	XP_011508605.1:n.-188-15277G>C
XR_922584.1:n.119-15277G>C
XR_922584.2:n.261-15277G>C