Canonical Allele Identifier: CA603029871

Gene: LINC02714

Linked Data

• dbSNP Id: rs1482579514
• gnomAD v2: 11-134626732-CA-C
• gnomAD v3: 11-134756838-CA-C
• gnomAD v4: 11-134756838-CA-C
• MyVariant Identifiers: chr11:g.134626733del (hg19) ; chr11:g.134756839del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134756839del , CM000673.2:g.134756839del	GRCh38
NC_000011.9:g.134626733del , CM000673.1:g.134626733del	GRCh37
NC_000011.8:g.134131943del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_147836.1:n.599-4235del