Canonical Allele Identifier: CA746282053
Gene: CDH4 HGNC NCBI

Linked Data

dbSNP Id: rs1223398052
gnomAD v3: 20-61531684-T-A
gnomAD v4: 20-61531684-T-A
MyVariant Identifiers: chr20:g.60106740T>A (hg19) chr20:g.61531684T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.61531684T>A , CM000682.2:g.61531684T>A GRCh38
NC_000020.10:g.60106740T>A , CM000682.1:g.60106740T>A GRCh37
NC_000020.9:g.59540135T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000614565.5:c.170-211879T>A MANE Select ENSP00000484928.1:n.170-211879T>A
ENST00000614565.4:c.170-211879T>A ENSP00000484928.1:n.170-211879T>A
NM_001252338.2:c.58+32192T>A NP_001239267.1:n.58+32192T>A
NM_001794.4:c.170-211879T>A NP_001785.2:n.170-211879T>A
NM_001794.5:c.170-211879T>A MANE Select NP_001785.2:n.170-211879T>A
Search 100 bp 5'
Search 100 bp 3'