Canonical Allele Identifier: CA746309450
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs1332471001
gnomAD v3: 20-61278835-G-C
gnomAD v4: 20-61278835-G-C
MyVariant Identifiers: chr20:g.59853891G>C (hg19) chr20:g.61278835G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61278835G>C , CM000682.2:g.61278835G>C GRCh38
NC_000020.10:g.59853891G>C , CM000682.1:g.59853891G>C GRCh37
NC_000020.9:g.59287286G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000614565.5:c.169+23898G>C MANE Select ENSP00000484928.1:n.169+23898G>C
ENST00000614565.4:c.169+23898G>C ENSP00000484928.1:n.169+23898G>C
NM_001794.4:c.169+23898G>C NP_001785.2:n.169+23898G>C
NM_001794.5:c.169+23898G>C MANE Select NP_001785.2:n.169+23898G>C
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