Canonical Allele Identifier: CA9616472
Gene: FPR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1056255
ClinVar RCV Id: RCV002242582
dbSNP Id: rs775451540
ExAC: 19:52249841 T / G
gnomAD v2: 19-52249841-T-G
gnomAD v3: 19-51746588-T-G
gnomAD v4: 19-51746588-T-G
MyVariant Identifiers: chr19:g.52249841T>G (hg19) chr19:g.51746588T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51746588T>G , CM000681.2:g.51746588T>G GRCh38
NC_000019.9:g.52249841T>G , CM000681.1:g.52249841T>G GRCh37
NC_000019.8:g.56941653T>G NCBI36
NG_023426.1:g.10310A>C , LRG_146:g.10310A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000594900.2:c.407A>C ENSP00000470750.2:p.His136Pro
ENST00000600815.2:c.407A>C ENSP00000472936.2:p.His136Pro
ENST00000304748.5:c.407A>C MANE Select ENSP00000302707.3:p.His136Pro
ENST00000304748.4:c.407A>C ENSP00000302707.3:p.His136Pro
ENST00000595042.5:c.407A>C ENSP00000471493.1:p.His136Pro
ENST00000600815.1:c.407A>C ENSP00000472936.1:p.His136Pro
NM_001193306.1:c.407A>C NP_001180235.1:p.His136Pro
NM_002029.3:c.407A>C , LRG_146t1:c.407A>C NP_002020.1:p.His136Pro
NM_001193306.2:c.407A>C NP_001180235.1:p.His136Pro
NM_002029.4:c.407A>C MANE Select NP_002020.1:p.His136Pro
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