Canonical Allele Identifier: CA224770961

Gene: LINC02757

Linked Data

• dbSNP Id: rs756326097
• MyVariant Identifiers: chr11:g.76332224del (hg19) ; chr11:g.76621180del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.76621182del , CM000673.2:g.76621182del	GRCh38
NC_000011.9:g.76332226del , CM000673.1:g.76332226del	GRCh37
NC_000011.8:g.76009874del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_247265.2:n.2147+4688del
XR_950334.1:n.2082+5393del
XR_001748311.1:n.2245+4688del
XR_001748312.1:n.1515+4688del