Canonical Allele Identifier: CA739092844
Gene: PTGFR HGNC NCBI

Linked Data

dbSNP Id: rs1220455624
gnomAD v3: 1-78490735-A-G
gnomAD v4: 1-78490735-A-G
MyVariant Identifiers: chr1:g.78956420A>G (hg19) chr1:g.78490735A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490735A>G , CM000663.2:g.78490735A>G GRCh38
NC_000001.10:g.78956420A>G , CM000663.1:g.78956420A>G GRCh37
NC_000001.9:g.78729008A>G NCBI36
NG_052997.1:g.4762A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370758.5:c.-72-1937A>G ENSP00000359794.1:n.-72-1937A>G
XM_006710781.2:c.-72-1937A>G XP_006710844.1:n.-72-1937A>G
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