Canonical Allele Identifier: CA317411354
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs574085378
gnomAD v3: 20-61531660-G-A
gnomAD v4: 20-61531660-G-A
MyVariant Identifiers: chr20:g.60106716G>A (hg19) chr20:g.61531660G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531660G>A , CM000682.2:g.61531660G>A GRCh38
NC_000020.10:g.60106716G>A , CM000682.1:g.60106716G>A GRCh37
NC_000020.9:g.59540111G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-211903G>A MANE Select ENSP00000484928.1:n.170-211903G>A
ENST00000614565.4:c.170-211903G>A ENSP00000484928.1:n.170-211903G>A
NM_001252338.2:c.58+32168G>A NP_001239267.1:n.58+32168G>A
NM_001794.4:c.170-211903G>A NP_001785.2:n.170-211903G>A
NM_001794.5:c.170-211903G>A MANE Select NP_001785.2:n.170-211903G>A
Search 100 bp 5'
Search 100 bp 3'