Canonical Allele Identifier: CA1177857851
Gene: PTGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490728G= , CM000663.2:g.78490728G= GRCh38
NC_000001.10:g.78956413G= , CM000663.1:g.78956413G= GRCh37
NC_000001.9:g.78729001G= NCBI36
NG_052997.1:g.4755G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370758.5:c.-72-1944G= ENSP00000359794.1:n.-72-1944G=
XM_006710781.2:c.-72-1944G= XP_006710844.1:n.-72-1944G=