Canonical Allele Identifier: CA623139838

Gene: CDH1

Linked Data

• dbSNP Id: rs1420525603
• gnomAD v2: 16-68771163-G-A
• gnomAD v4: 16-68737260-G-A
• MyVariant Identifiers: chr16:g.68771163G>A (hg19) ; chr16:g.68737260G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737260G>A , CM000678.2:g.68737260G>A	GRCh38
NC_000016.9:g.68771163G>A , CM000678.1:g.68771163G>A	GRCh37
NC_000016.8:g.67328664G>A	NCBI36
NG_008021.1:g.4969G>A , LRG_301:g.4969G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.9:c.-156G>A	ENSP00000261769.4:n.-156G>A