Canonical Allele Identifier: CA1177857843
Gene: PTGFR HGNC NCBI

Linked Data

dbSNP Id: rs1649366169

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490708_78490715del , CM000663.2:g.78490708_78490715del GRCh38
NC_000001.10:g.78956393_78956400del , CM000663.1:g.78956393_78956400del GRCh37
NC_000001.9:g.78728981_78728988del NCBI36
NG_052997.1:g.4735_4742del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370758.5:c.-72-1964_-72-1957del ENSP00000359794.1:n.-72-1964_-72-1957del
XM_006710781.2:c.-72-1964_-72-1957del XP_006710844.1:n.-72-1964_-72-1957del