Canonical Allele Identifier: CA723156413
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1157212868
gnomAD v3: 16-68737243-G-A
gnomAD v4: 16-68737243-G-A
MyVariant Identifiers: chr16:g.68771146G>A (hg19) chr16:g.68737243G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737243G>A , CM000678.2:g.68737243G>A GRCh38
NC_000016.9:g.68771146G>A , CM000678.1:g.68771146G>A GRCh37
NC_000016.8:g.67328647G>A NCBI36
NG_008021.1:g.4952G>A , LRG_301:g.4952G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.9:c.-173G>A ENSP00000261769.4:n.-173G>A
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