Canonical Allele Identifier: CA1143866058
Gene: PTGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490575T= , CM000663.2:g.78490575T= GRCh38
NC_000001.10:g.78956260T= , CM000663.1:g.78956260T= GRCh37
NC_000001.9:g.78728848T= NCBI36
NG_052997.1:g.4602T=

Transcript Alleles

HGVS Amino-acid change
ENST00000370758.5:c.-72-2097T= ENSP00000359794.1:n.-72-2097T=
XM_006710781.2:c.-72-2097T= XP_006710844.1:n.-72-2097T=