Canonical Allele Identifier: CA224770970

Gene: LINC02757

Linked Data

• dbSNP Id: rs1032166081
• MyVariant Identifiers: chr11:g.76332241T>C (hg19) ; chr11:g.76621197T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.76621197T>C , CM000673.2:g.76621197T>C	GRCh38
NC_000011.9:g.76332241T>C , CM000673.1:g.76332241T>C	GRCh37
NC_000011.8:g.76009889T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_247265.2:n.2147+4671A>G
XR_950334.1:n.2082+5376A>G
XR_001748311.1:n.2245+4671A>G
XR_001748312.1:n.1515+4671A>G