Canonical Allele Identifier: CA746282031
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs1422154901
gnomAD v3: 20-61531638-T-C
gnomAD v4: 20-61531638-T-C
MyVariant Identifiers: chr20:g.60106694T>C (hg19) chr20:g.61531638T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531638T>C , CM000682.2:g.61531638T>C GRCh38
NC_000020.10:g.60106694T>C , CM000682.1:g.60106694T>C GRCh37
NC_000020.9:g.59540089T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-211925T>C MANE Select ENSP00000484928.1:n.170-211925T>C
ENST00000614565.4:c.170-211925T>C ENSP00000484928.1:n.170-211925T>C
NM_001252338.2:c.58+32146T>C NP_001239267.1:n.58+32146T>C
NM_001794.4:c.170-211925T>C NP_001785.2:n.170-211925T>C
NM_001794.5:c.170-211925T>C MANE Select NP_001785.2:n.170-211925T>C
Search 100 bp 5'
Search 100 bp 3'