Canonical Allele Identifier: CA471301620
Gene: PTGES3P4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104605423C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102845666C>T , CM000672.2:g.102845666C>T GRCh38
NC_000010.10:g.104605423C>T , CM000672.1:g.104605423C>T GRCh37
NC_000010.9:g.104595413C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000426243.2:n.72C>T