Canonical Allele Identifier: CA283273053
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs983997602
gnomAD v3: 16-68737251-G-T
gnomAD v4: 16-68737251-G-T
MyVariant Identifiers: chr16:g.68771154G>T (hg19) chr16:g.68737251G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737251G>T , CM000678.2:g.68737251G>T GRCh38
NC_000016.9:g.68771154G>T , CM000678.1:g.68771154G>T GRCh37
NC_000016.8:g.67328655G>T NCBI36
NG_008021.1:g.4960G>T , LRG_301:g.4960G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.9:c.-165G>T ENSP00000261769.4:n.-165G>T
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