Canonical Allele Identifier: CA680386987

Gene: LINC02757

Linked Data

• dbSNP Id: rs1427261841
• gnomAD v3: 11-76621167-A-G
• gnomAD v4: 11-76621167-A-G
• MyVariant Identifiers: chr11:g.76332211A>G (hg19) ; chr11:g.76621167A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.76621167A>G , CM000673.2:g.76621167A>G	GRCh38
NC_000011.9:g.76332211A>G , CM000673.1:g.76332211A>G	GRCh37
NC_000011.8:g.76009859A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_247265.2:n.2147+4701T>C
XR_950334.1:n.2082+5406T>C
XR_001748311.1:n.2245+4701T>C
XR_001748312.1:n.1515+4701T>C