Canonical Allele Identifier: CA1177857792
Gene: PTGFR HGNC NCBI

Linked Data

dbSNP Id: rs1649362078
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490582G>A , CM000663.2:g.78490582G>A GRCh38
NC_000001.10:g.78956267G>A , CM000663.1:g.78956267G>A GRCh37
NC_000001.9:g.78728855G>A NCBI36
NG_052997.1:g.4609G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370758.5:c.-72-2090G>A ENSP00000359794.1:n.-72-2090G>A
XM_006710781.2:c.-72-2090G>A XP_006710844.1:n.-72-2090G>A
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