Canonical Allele Identifier: CA1006134507
Gene: PTGFRN HGNC NCBI

Linked Data

dbSNP Id: rs1649622801
gnomAD v3: 1-116925216-C-A
gnomAD v4: 1-116925216-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.116925216C>A , CM000663.2:g.116925216C>A GRCh38
NC_000001.10:g.117467838C>A , CM000663.1:g.117467838C>A GRCh37
NC_000001.9:g.117269361C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393203.3:c.49+14964C>A MANE Select ENSP00000376899.2:n.49+14964C>A
ENST00000393203.2:c.49+14964C>A ENSP00000376899.2:n.49+14964C>A
NM_020440.3:c.49+14964C>A NP_065173.2:n.49+14964C>A
NM_020440.4:c.49+14964C>A MANE Select NP_065173.2:n.49+14964C>A
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