Canonical Allele Identifier: CA603029893

Gene: LINC02714

Linked Data

• dbSNP Id: rs1310897101
• gnomAD v2: 11-134626918-G-A
• gnomAD v3: 11-134757024-G-A
• gnomAD v4: 11-134757024-G-A
• MyVariant Identifiers: chr11:g.134626918G>A (hg19) ; chr11:g.134757024G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134757024G>A , CM000673.2:g.134757024G>A	GRCh38
NC_000011.9:g.134626918G>A , CM000673.1:g.134626918G>A	GRCh37
NC_000011.8:g.134132128G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_147836.1:n.599-4050G>A