Canonical Allele Identifier: CA14764080
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs4925189
gnomAD v2: 20-59947044-G-A
gnomAD v3: 20-61371988-G-A
gnomAD v4: 20-61371988-G-A
MyVariant Identifiers: chr20:g.59947044G>A (hg19) chr20:g.61371988G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61371988G>A , CM000682.2:g.61371988G>A GRCh38
NC_000020.10:g.59947044G>A , CM000682.1:g.59947044G>A GRCh37
NC_000020.9:g.59380439G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000614565.5:c.169+117051G>A MANE Select ENSP00000484928.1:n.169+117051G>A
ENST00000614565.4:c.169+117051G>A ENSP00000484928.1:n.169+117051G>A
NM_001794.4:c.169+117051G>A NP_001785.2:n.169+117051G>A
NM_001794.5:c.169+117051G>A MANE Select NP_001785.2:n.169+117051G>A
Search 100 bp 5'
Search 100 bp 3'