ClinGen Allele Registry
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Canonical Allele Identifier:
CA15634965
Gene: PTGES3P4
HGNC
NCBI
Linked Data
dbSNP Id:
rs17724534
gnomAD v2:
10-104605521-C-T
gnomAD v3:
10-102845764-C-T
gnomAD v4:
10-102845764-C-T
MyVariant Identifiers:
chr10:g.104605521C>T (hg19)
chr10:g.102845764C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.102845764C>T , CM000672.2:g.102845764C>T
GRCh38
NC_000010.10:g.104605521C>T , CM000672.1:g.104605521C>T
GRCh37
NC_000010.9:g.104595511C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000426243.2:n.170C>T
Search 100 bp 5'
Search 100 bp 3'