Canonical Allele Identifier: CA1003503341
Gene: PTGFR HGNC NCBI

Linked Data

dbSNP Id: rs1409256218
gnomAD v3: 1-78490584-G-C
gnomAD v4: 1-78490584-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490584G>C , CM000663.2:g.78490584G>C GRCh38
NC_000001.10:g.78956269G>C , CM000663.1:g.78956269G>C GRCh37
NC_000001.9:g.78728857G>C NCBI36
NG_052997.1:g.4611G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370758.5:c.-72-2088G>C ENSP00000359794.1:n.-72-2088G>C
XM_006710781.2:c.-72-2088G>C XP_006710844.1:n.-72-2088G>C
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