Canonical Allele Identifier: CA224770959

Gene: LINC02757

Linked Data

• dbSNP Id: rs34970541
• MyVariant Identifiers: chr11:g.76332216_76332217insT (hg19) ; chr11:g.76621172_76621173insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.76621176dup , CM000673.2:g.76621176dup	GRCh38
NC_000011.9:g.76332220dup , CM000673.1:g.76332220dup	GRCh37
NC_000011.8:g.76009868dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_247265.2:n.2147+4695dup
XR_950334.1:n.2082+5400dup
XR_001748311.1:n.2245+4695dup
XR_001748312.1:n.1515+4695dup