Canonical Allele Identifier: CA9616451
Gene: FPR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2192186
ClinVar RCV Id: RCV002620980
dbSNP Id: rs774585820
ExAC: 19:52249742 C / T
gnomAD v2: 19-52249742-C-T
gnomAD v4: 19-51746489-C-T
COSMIC: COSM5856532
MyVariant Identifiers: chr19:g.52249742C>T (hg19) chr19:g.51746489C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51746489C>T , CM000681.2:g.51746489C>T GRCh38
NC_000019.9:g.52249742C>T , CM000681.1:g.52249742C>T GRCh37
NC_000019.8:g.56941554C>T NCBI36
NG_023426.1:g.10409G>A , LRG_146:g.10409G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000594900.2:c.506G>A ENSP00000470750.2:p.Gly169Asp
ENST00000600815.2:c.506G>A ENSP00000472936.2:p.Gly169Asp
ENST00000304748.5:c.506G>A MANE Select ENSP00000302707.3:p.Gly169Asp
ENST00000304748.4:c.506G>A ENSP00000302707.3:p.Gly169Asp
ENST00000595042.5:c.506G>A ENSP00000471493.1:p.Gly169Asp
ENST00000600815.1:c.506G>A ENSP00000472936.1:p.Gly169Asp
NM_001193306.1:c.506G>A NP_001180235.1:p.Gly169Asp
NM_002029.3:c.506G>A , LRG_146t1:c.506G>A NP_002020.1:p.Gly169Asp
NM_001193306.2:c.506G>A NP_001180235.1:p.Gly169Asp
NM_002029.4:c.506G>A MANE Select NP_002020.1:p.Gly169Asp
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