Canonical Allele Identifier: CA623139839
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1476949230
gnomAD v2: 16-68771165-T-C
gnomAD v3: 16-68737262-T-C
gnomAD v4: 16-68737262-T-C
MyVariant Identifiers: chr16:g.68771165T>C (hg19) chr16:g.68737262T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737262T>C , CM000678.2:g.68737262T>C GRCh38
NC_000016.9:g.68771165T>C , CM000678.1:g.68771165T>C GRCh37
NC_000016.8:g.67328666T>C NCBI36
NG_008021.1:g.4971T>C , LRG_301:g.4971T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.9:c.-154T>C ENSP00000261769.4:n.-154T>C
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