Canonical Allele Identifier: CA731228571

Gene: LINC02775

Linked Data

• dbSNP Id: rs1190402881
• MyVariant Identifiers: chr1:g.214261017_214261021del (hg19) ; chr1:g.214087674_214087678del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214087675_214087679del , CM000663.2:g.214087675_214087679del	GRCh38
NC_000001.10:g.214261018_214261022del , CM000663.1:g.214261018_214261022del	GRCh37
NC_000001.9:g.212327641_212327645del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510303.1:c.-188-15240_-188-15236del	XP_011508605.1:n.-188-15240_-188-15236del
XR_922584.1:n.119-15240_119-15236del
XR_922584.2:n.261-15240_261-15236del