Canonical Allele Identifier: CA9616481
Gene: FPR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2729628
ClinVar RCV Id: RCV003596803
dbSNP Id: rs190373580
ExAC: 19:52249896 G / C
gnomAD v2: 19-52249896-G-C
gnomAD v3: 19-51746643-G-C
gnomAD v4: 19-51746643-G-C
MyVariant Identifiers: chr19:g.52249896G>C (hg19) chr19:g.51746643G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51746643G>C , CM000681.2:g.51746643G>C GRCh38
NC_000019.9:g.52249896G>C , CM000681.1:g.52249896G>C GRCh37
NC_000019.8:g.56941708G>C NCBI36
NG_023426.1:g.10255C>G , LRG_146:g.10255C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000594900.2:c.352C>G ENSP00000470750.2:p.Leu118Val
ENST00000600815.2:c.352C>G ENSP00000472936.2:p.Leu118Val
ENST00000304748.5:c.352C>G MANE Select ENSP00000302707.3:p.Leu118Val
ENST00000304748.4:c.352C>G ENSP00000302707.3:p.Leu118Val
ENST00000595042.5:c.352C>G ENSP00000471493.1:p.Leu118Val
ENST00000600815.1:c.352C>G ENSP00000472936.1:p.Leu118Val
NM_001193306.1:c.352C>G NP_001180235.1:p.Leu118Val
NM_002029.3:c.352C>G , LRG_146t1:c.352C>G NP_002020.1:p.Leu118Val
NM_001193306.2:c.352C>G NP_001180235.1:p.Leu118Val
NM_002029.4:c.352C>G MANE Select NP_002020.1:p.Leu118Val
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