Canonical Allele Identifier: CA1177857787
Gene: PTGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490578G= , CM000663.2:g.78490578G= GRCh38
NC_000001.10:g.78956263G= , CM000663.1:g.78956263G= GRCh37
NC_000001.9:g.78728851G= NCBI36
NG_052997.1:g.4605G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370758.5:c.-72-2094G= ENSP00000359794.1:n.-72-2094G=
XM_006710781.2:c.-72-2094G= XP_006710844.1:n.-72-2094G=