Canonical Allele Identifier: CA1003503361
Gene: PTGFR HGNC NCBI

Linked Data

dbSNP Id: rs1649362886
gnomAD v3: 1-78490618-C-T
gnomAD v4: 1-78490618-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490618C>T , CM000663.2:g.78490618C>T GRCh38
NC_000001.10:g.78956303C>T , CM000663.1:g.78956303C>T GRCh37
NC_000001.9:g.78728891C>T NCBI36
NG_052997.1:g.4645C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370758.5:c.-72-2054C>T ENSP00000359794.1:n.-72-2054C>T
XM_006710781.2:c.-72-2054C>T XP_006710844.1:n.-72-2054C>T