Canonical Allele Identifier: CA1177857861
Gene: PTGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490747T>A , CM000663.2:g.78490747T>A GRCh38
NC_000001.10:g.78956432T>A , CM000663.1:g.78956432T>A GRCh37
NC_000001.9:g.78729020T>A NCBI36
NG_052997.1:g.4774T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370758.5:c.-72-1925T>A ENSP00000359794.1:n.-72-1925T>A
XM_006710781.2:c.-72-1925T>A XP_006710844.1:n.-72-1925T>A