Canonical Allele Identifier: CA1177857841
Gene: PTGFR HGNC NCBI

Linked Data

dbSNP Id: rs1557644407

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490707T>C , CM000663.2:g.78490707T>C GRCh38
NC_000001.10:g.78956392T>C , CM000663.1:g.78956392T>C GRCh37
NC_000001.9:g.78728980T>C NCBI36
NG_052997.1:g.4734T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370758.5:c.-72-1965T>C ENSP00000359794.1:n.-72-1965T>C
XM_006710781.2:c.-72-1965T>C XP_006710844.1:n.-72-1965T>C