ClinGen Allele Registry
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Canonical Allele Identifier:
CA337770287
Gene: PUDPP1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.15396457T>C
GRCh37
chrY:g.17508337T>C
Linked Data - NCBI & NCI
dbSNP:
17222419
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.15396457T>C , CM000686.2:g.15396457T>C
GRCh38
NC_000024.9:g.17508337T>C , CM000686.1:g.17508337T>C
GRCh37
NC_000024.8:g.16017731T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000421058.1:n.41-14615A>G
Search 100 bp 5'
Search 100 bp 3'