Canonical Allele Identifier: CA603029887

Gene: LINC02714

Linked Data

• dbSNP Id: rs1397738845
• gnomAD v2: 11-134626889-C-T
• gnomAD v3: 11-134756995-C-T
• gnomAD v4: 11-134756995-C-T
• MyVariant Identifiers: chr11:g.134626889C>T (hg19) ; chr11:g.134756995C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134756995C>T , CM000673.2:g.134756995C>T	GRCh38
NC_000011.9:g.134626889C>T , CM000673.1:g.134626889C>T	GRCh37
NC_000011.8:g.134132099C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_147836.1:n.599-4079C>T