Canonical Allele Identifier: CA224770973

Gene: LINC02757

Linked Data

• dbSNP Id: rs996211438
• gnomAD v3: 11-76621204-T-C
• gnomAD v4: 11-76621204-T-C
• MyVariant Identifiers: chr11:g.76332248T>C (hg19) ; chr11:g.76621204T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.76621204T>C , CM000673.2:g.76621204T>C	GRCh38
NC_000011.9:g.76332248T>C , CM000673.1:g.76332248T>C	GRCh37
NC_000011.8:g.76009896T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_247265.2:n.2147+4664A>G
XR_950334.1:n.2082+5369A>G
XR_001748311.1:n.2245+4664A>G
XR_001748312.1:n.1515+4664A>G