Canonical Allele Identifier: CA232144092

Gene: LINC02714

Linked Data

• dbSNP Id: rs918853526
• gnomAD v2: 11-134626707-A-C
• gnomAD v3: 11-134756813-A-C
• gnomAD v4: 11-134756813-A-C
• MyVariant Identifiers: chr11:g.134626707A>C (hg19) ; chr11:g.134756813A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134756813A>C , CM000673.2:g.134756813A>C	GRCh38
NC_000011.9:g.134626707A>C , CM000673.1:g.134626707A>C	GRCh37
NC_000011.8:g.134131917A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_147836.1:n.599-4261A>C