Canonical Allele Identifier: CA1012083070

Gene: LINC02775

Linked Data

• dbSNP Id: rs1665557789
• gnomAD v3: 1-214087954-C-CT
• gnomAD v4: 1-214087954-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214087955dup , CM000663.2:g.214087955dup	GRCh38
NC_000001.10:g.214261298dup , CM000663.1:g.214261298dup	GRCh37
NC_000001.9:g.212327921dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510303.1:c.-188-15517dup	XP_011508605.1:n.-188-15517dup
XR_922584.1:n.119-15517dup
XR_922584.2:n.261-15517dup