Canonical Allele Identifier: CA603029888

Gene: LINC02714

Linked Data

• dbSNP Id: rs1304628954
• gnomAD v2: 11-134626912-G-A
• gnomAD v3: 11-134757018-G-A
• gnomAD v4: 11-134757018-G-A
• MyVariant Identifiers: chr11:g.134626912G>A (hg19) ; chr11:g.134757018G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134757018G>A , CM000673.2:g.134757018G>A	GRCh38
NC_000011.9:g.134626912G>A , CM000673.1:g.134626912G>A	GRCh37
NC_000011.8:g.134132122G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_147836.1:n.599-4056G>A