Canonical Allele Identifier: CA673875032

Gene: LINC02714

Linked Data

• dbSNP Id: rs1289780056
• gnomAD v3: 11-134757051-G-T
• gnomAD v4: 11-134757051-G-T
• MyVariant Identifiers: chr11:g.134626945G>T (hg19) ; chr11:g.134757051G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134757051G>T , CM000673.2:g.134757051G>T	GRCh38
NC_000011.9:g.134626945G>T , CM000673.1:g.134626945G>T	GRCh37
NC_000011.8:g.134132155G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_147836.1:n.599-4023G>T