Canonical Allele Identifier: CA10648757
Gene: CDH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 320206
ClinVar RCV Id: RCV000308578
dbSNP Id: rs11440411

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68644751dup , CM000678.2:g.68644751dup GRCh38
NC_000016.9:g.68678654dup , CM000678.1:g.68678654dup GRCh37
NC_000016.8:g.67236155dup NCBI36
NG_009096.1:g.5504dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000565453.1:n.223-258dup
NM_001793.4:c.-629dup NP_001784.2:n.-629dup