Canonical Allele Identifier: CA471301742
Gene: PTGES3P4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104605442A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102845685A>T , CM000672.2:g.102845685A>T GRCh38
NC_000010.10:g.104605442A>T , CM000672.1:g.104605442A>T GRCh37
NC_000010.9:g.104595432A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000426243.2:n.91A>T