Canonical Allele Identifier: CA683615343

Gene: LINC02356

Linked Data

• dbSNP Id: rs1206641966
• gnomAD v3: 12-111399113-AG-A
• gnomAD v4: 12-111399113-AG-A
• MyVariant Identifiers: chr12:g.111836918del (hg19) ; chr12:g.111399114del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111399116del , CM000674.2:g.111399116del	GRCh38
NC_000012.11:g.111836920del , CM000674.1:g.111836920del	GRCh37
NC_000012.10:g.110321303del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+2243del