Canonical Allele Identifier: CA471301757
Gene: PTGES3P4 HGNC NCBI

Linked Data

dbSNP Id: rs1017923112
MyVariant Identifiers: chr10:g.104605446C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102845689C>A , CM000672.2:g.102845689C>A GRCh38
NC_000010.10:g.104605446C>A , CM000672.1:g.104605446C>A GRCh37
NC_000010.9:g.104595436C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000426243.2:n.95C>A