Canonical Allele Identifier: CA283273052
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs936851477
gnomAD v3: 16-68737248-G-A
gnomAD v4: 16-68737248-G-A
MyVariant Identifiers: chr16:g.68737248G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737248G>A , CM000678.2:g.68737248G>A GRCh38
NC_000016.9:g.68771151G>A , CM000678.1:g.68771151G>A GRCh37
NC_000016.8:g.67328652G>A NCBI36
NG_008021.1:g.4957G>A , LRG_301:g.4957G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.9:c.-168G>A ENSP00000261769.4:n.-168G>A
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