Canonical Allele Identifier: CA10644092

Gene: CDH3

Linked Data

• ClinVar Variation Id: 320209
• ClinVar RCV Id: RCV000314275
• dbSNP Id: rs886052224
• gnomAD v2: 16-68678649-A-AG
• gnomAD v3: 16-68644746-A-AG
• gnomAD v4: 16-68644746-A-AG
• MyVariant Identifiers: chr16:g.68678649_68678650insG (hg19) ; chr16:g.68644746_68644747insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68644746_68644747insG , CM000678.2:g.68644746_68644747insG	GRCh38
NC_000016.9:g.68678649_68678650insG , CM000678.1:g.68678649_68678650insG	GRCh37
NC_000016.8:g.67236150_67236151insG	NCBI36
NG_009096.1:g.5499_5500insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565453.1:n.223-263_223-262insG
NM_001793.4:c.-634_-633insG	NP_001784.2:n.-634_-633insG