Canonical Allele Identifier: CA1191227438
Gene: PTGFRN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.116925208G= , CM000663.2:g.116925208G= GRCh38
NC_000001.10:g.117467830G= , CM000663.1:g.117467830G= GRCh37
NC_000001.9:g.117269353G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393203.3:c.49+14956G= MANE Select ENSP00000376899.2:n.49+14956G=
ENST00000393203.2:c.49+14956G= ENSP00000376899.2:n.49+14956G=
NM_020440.3:c.49+14956G= NP_065173.2:n.49+14956G=
NM_020440.4:c.49+14956G= MANE Select NP_065173.2:n.49+14956G=
Search 100 bp 5'
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