Canonical Allele Identifier: CA673874920

Gene: LINC02714

Linked Data

• dbSNP Id: rs562875713
• gnomAD v3: 11-134756943-T-C
• gnomAD v4: 11-134756943-T-C
• MyVariant Identifiers: chr11:g.134626837T>C (hg19) ; chr11:g.134756943T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134756943T>C , CM000673.2:g.134756943T>C	GRCh38
NC_000011.9:g.134626837T>C , CM000673.1:g.134626837T>C	GRCh37
NC_000011.8:g.134132047T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_147836.1:n.599-4131T>C