Canonical Allele Identifier: CA1177857852
Gene: PTGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490731A= , CM000663.2:g.78490731A= GRCh38
NC_000001.10:g.78956416A= , CM000663.1:g.78956416A= GRCh37
NC_000001.9:g.78729004A= NCBI36
NG_052997.1:g.4758A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370758.5:c.-72-1941A= ENSP00000359794.1:n.-72-1941A=
XM_006710781.2:c.-72-1941A= XP_006710844.1:n.-72-1941A=