Canonical Allele Identifier: CA1177857799
Gene: PTGFR HGNC NCBI

Linked Data

dbSNP Id: rs1649362733
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490612G>T , CM000663.2:g.78490612G>T GRCh38
NC_000001.10:g.78956297G>T , CM000663.1:g.78956297G>T GRCh37
NC_000001.9:g.78728885G>T NCBI36
NG_052997.1:g.4639G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370758.5:c.-72-2060G>T ENSP00000359794.1:n.-72-2060G>T
XM_006710781.2:c.-72-2060G>T XP_006710844.1:n.-72-2060G>T
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