Canonical Allele Identifier: CA723156434
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1282368601
gnomAD v3: 16-68737264-A-T
gnomAD v4: 16-68737264-A-T
MyVariant Identifiers: chr16:g.68771167A>T (hg19) chr16:g.68737264A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737264A>T , CM000678.2:g.68737264A>T GRCh38
NC_000016.9:g.68771167A>T , CM000678.1:g.68771167A>T GRCh37
NC_000016.8:g.67328668A>T NCBI36
NG_008021.1:g.4973A>T , LRG_301:g.4973A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.9:c.-152A>T ENSP00000261769.4:n.-152A>T
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