Canonical Allele Identifier: CA471301638
Gene: PTGES3P4 HGNC NCBI

Linked Data

dbSNP Id: rs1844288012
MyVariant Identifiers: chr10:g.104605426G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102845669G>A , CM000672.2:g.102845669G>A GRCh38
NC_000010.10:g.104605426G>A , CM000672.1:g.104605426G>A GRCh37
NC_000010.9:g.104595416G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000426243.2:n.75G>A