ClinGen Allele Registry
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Canonical Allele Identifier:
CA337631275
Gene: CDY3P
HGNC
NCBI
Linked Data
dbSNP Id:
rs13304043
gnomAD v3:
Y-9167312-G-A
gnomAD v4:
Y-9167312-G-A
MyVariant Identifiers:
chrY:g.9004921G>A (hg19)
chrY:g.9167312G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.9167312G>A , CM000686.2:g.9167312G>A
GRCh38
NC_000024.9:g.9004921G>A , CM000686.1:g.9004921G>A
GRCh37
NC_000024.8:g.9064921G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000454543.1:n.391C>T
Search 100 bp 5'
Search 100 bp 3'