Canonical Allele Identifier: CA731228609

Gene: LINC02775

Linked Data

• dbSNP Id: rs1327588005
• gnomAD v3: 1-214087712-TC-T
• gnomAD v4: 1-214087712-TC-T
• MyVariant Identifiers: chr1:g.214261056del (hg19) ; chr1:g.214087713del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214087713del , CM000663.2:g.214087713del	GRCh38
NC_000001.10:g.214261056del , CM000663.1:g.214261056del	GRCh37
NC_000001.9:g.212327679del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510303.1:c.-188-15275del	XP_011508605.1:n.-188-15275del
XR_922584.1:n.119-15275del
XR_922584.2:n.261-15275del