Canonical Allele Identifier: CA25440554
Gene: PTGFR HGNC NCBI

Linked Data

dbSNP Id: rs1020574577
MyVariant Identifiers: chr1:g.78956274T>C (hg19) chr1:g.78490589T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490589T>C , CM000663.2:g.78490589T>C GRCh38
NC_000001.10:g.78956274T>C , CM000663.1:g.78956274T>C GRCh37
NC_000001.9:g.78728862T>C NCBI36
NG_052997.1:g.4616T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370758.5:c.-72-2083T>C ENSP00000359794.1:n.-72-2083T>C
XM_006710781.2:c.-72-2083T>C XP_006710844.1:n.-72-2083T>C
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