Canonical Allele Identifier: CA1006134525
Gene: PTGFRN HGNC NCBI

Linked Data

dbSNP Id: rs1649623505
gnomAD v3: 1-116925240-C-CA
gnomAD v4: 1-116925240-C-CA
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.116925242dup , CM000663.2:g.116925242dup GRCh38
NC_000001.10:g.117467864dup , CM000663.1:g.117467864dup GRCh37
NC_000001.9:g.117269387dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393203.3:c.49+14990dup MANE Select ENSP00000376899.2:n.49+14990dup
ENST00000393203.2:c.49+14990dup ENSP00000376899.2:n.49+14990dup
NM_020440.3:c.49+14990dup NP_065173.2:n.49+14990dup
NM_020440.4:c.49+14990dup MANE Select NP_065173.2:n.49+14990dup
Search 100 bp 5'
Search 100 bp 3'