Canonical Allele Identifier: CA1006134527
Gene: PTGFRN HGNC NCBI

Linked Data

dbSNP Id: rs1649623785
gnomAD v3: 1-116925261-T-C
gnomAD v4: 1-116925261-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.116925261T>C , CM000663.2:g.116925261T>C GRCh38
NC_000001.10:g.117467883T>C , CM000663.1:g.117467883T>C GRCh37
NC_000001.9:g.117269406T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393203.3:c.49+15009T>C MANE Select ENSP00000376899.2:n.49+15009T>C
ENST00000393203.2:c.49+15009T>C ENSP00000376899.2:n.49+15009T>C
NM_020440.3:c.49+15009T>C NP_065173.2:n.49+15009T>C
NM_020440.4:c.49+15009T>C MANE Select NP_065173.2:n.49+15009T>C
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