Canonical Allele Identifier: CA603029894

Gene: LINC02714

Linked Data

• dbSNP Id: rs1242956116
• gnomAD v2: 11-134626919-C-G
• gnomAD v3: 11-134757025-C-G
• gnomAD v4: 11-134757025-C-G
• MyVariant Identifiers: chr11:g.134626919C>G (hg19) ; chr11:g.134757025C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134757025C>G , CM000673.2:g.134757025C>G	GRCh38
NC_000011.9:g.134626919C>G , CM000673.1:g.134626919C>G	GRCh37
NC_000011.8:g.134132129C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_147836.1:n.599-4049C>G