Canonical Allele Identifier: CA524020874
Gene: PTGFR HGNC NCBI

Linked Data

dbSNP Id: rs1407695598
gnomAD v2: 1-78956400-G-C
MyVariant Identifiers: chr1:g.78956400G>C (hg19) chr1:g.78490715G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490715G>C , CM000663.2:g.78490715G>C GRCh38
NC_000001.10:g.78956400G>C , CM000663.1:g.78956400G>C GRCh37
NC_000001.9:g.78728988G>C NCBI36
NG_052997.1:g.4742G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370758.5:c.-72-1957G>C ENSP00000359794.1:n.-72-1957G>C
XM_006710781.2:c.-72-1957G>C XP_006710844.1:n.-72-1957G>C
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