Canonical Allele Identifier: CA680386992

Gene: LINC02757

Linked Data

• dbSNP Id: rs1197023830
• MyVariant Identifiers: chr11:g.76332233G>C (hg19) ; chr11:g.76621189G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.76621189G>C , CM000673.2:g.76621189G>C	GRCh38
NC_000011.9:g.76332233G>C , CM000673.1:g.76332233G>C	GRCh37
NC_000011.8:g.76009881G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_247265.2:n.2147+4679C>G
XR_950334.1:n.2082+5384C>G
XR_001748311.1:n.2245+4679C>G
XR_001748312.1:n.1515+4679C>G