Canonical Allele Identifier: CA9616478
Gene: FPR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1398802
ClinVar RCV Id: RCV001922654
dbSNP Id: rs764940294
ExAC: 19:52249881 G / A
gnomAD v2: 19-52249881-G-A
gnomAD v3: 19-51746628-G-A
gnomAD v4: 19-51746628-G-A
COSMIC: COSM1304982
MyVariant Identifiers: chr19:g.52249881G>A (hg19) chr19:g.51746628G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51746628G>A , CM000681.2:g.51746628G>A GRCh38
NC_000019.9:g.52249881G>A , CM000681.1:g.52249881G>A GRCh37
NC_000019.8:g.56941693G>A NCBI36
NG_023426.1:g.10270C>T , LRG_146:g.10270C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000594900.2:c.367C>T ENSP00000470750.2:p.Arg123Cys
ENST00000600815.2:c.367C>T ENSP00000472936.2:p.Arg123Cys
ENST00000304748.5:c.367C>T MANE Select ENSP00000302707.3:p.Arg123Cys
ENST00000304748.4:c.367C>T ENSP00000302707.3:p.Arg123Cys
ENST00000595042.5:c.367C>T ENSP00000471493.1:p.Arg123Cys
ENST00000600815.1:c.367C>T ENSP00000472936.1:p.Arg123Cys
NM_001193306.1:c.367C>T NP_001180235.1:p.Arg123Cys
NM_002029.3:c.367C>T , LRG_146t1:c.367C>T NP_002020.1:p.Arg123Cys
NM_001193306.2:c.367C>T NP_001180235.1:p.Arg123Cys
NM_002029.4:c.367C>T MANE Select NP_002020.1:p.Arg123Cys
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