Canonical Allele Identifier: CA2486143441

Gene: LINC02775

Linked Data

• dbSNP Id: rs1665554329

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214087641_214087653del , CM000663.2:g.214087641_214087653del	GRCh38
NC_000001.10:g.214260984_214260996del , CM000663.1:g.214260984_214260996del	GRCh37
NC_000001.9:g.212327607_212327619del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510303.1:c.-188-15211_-188-15199del	XP_011508605.1:n.-188-15211_-188-15199del
XR_922584.1:n.119-15211_119-15199del
XR_922584.2:n.261-15211_261-15199del