Canonical Allele Identifier: CA317225636
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs553515969
gnomAD v2: 20-59853895-G-A
gnomAD v3: 20-61278839-G-A
gnomAD v4: 20-61278839-G-A
MyVariant Identifiers: chr20:g.59853895G>A (hg19) chr20:g.61278839G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61278839G>A , CM000682.2:g.61278839G>A GRCh38
NC_000020.10:g.59853895G>A , CM000682.1:g.59853895G>A GRCh37
NC_000020.9:g.59287290G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000614565.5:c.169+23902G>A MANE Select ENSP00000484928.1:n.169+23902G>A
ENST00000614565.4:c.169+23902G>A ENSP00000484928.1:n.169+23902G>A
NM_001794.4:c.169+23902G>A NP_001785.2:n.169+23902G>A
NM_001794.5:c.169+23902G>A MANE Select NP_001785.2:n.169+23902G>A
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