Canonical Allele Identifier: CA471301641
Gene: PTGES3P4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104605427C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102845670C>G , CM000672.2:g.102845670C>G GRCh38
NC_000010.10:g.104605427C>G , CM000672.1:g.104605427C>G GRCh37
NC_000010.9:g.104595417C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000426243.2:n.76C>G