Canonical Allele Identifier: CA673875017

Gene: LINC02714

Linked Data

• dbSNP Id: rs1487823772
• MyVariant Identifiers: chr11:g.134626917T>C (hg19) ; chr11:g.134757023T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134757023T>C , CM000673.2:g.134757023T>C	GRCh38
NC_000011.9:g.134626917T>C , CM000673.1:g.134626917T>C	GRCh37
NC_000011.8:g.134132127T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_147836.1:n.599-4051T>C