Canonical Allele Identifier: CA232144122

Gene: LINC02714

Linked Data

• dbSNP Id: rs78326128
• MyVariant Identifiers: chr11:g.134626916T>G (hg19) ; chr11:g.134757022T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134757022T>G , CM000673.2:g.134757022T>G	GRCh38
NC_000011.9:g.134626916T>G , CM000673.1:g.134626916T>G	GRCh37
NC_000011.8:g.134132126T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_147836.1:n.599-4052T>G