Canonical Allele Identifier: CA9616429

Gene: FPR1

Linked Data

• ClinVar Variation Id: 1168164
• ClinVar RCV Id: RCV001824979 ; RCV002241361
• dbSNP Id: rs1042229
• ExAC: 19:52249672 A / G
• gnomAD v2: 19-52249672-A-G
• gnomAD v3: 19-51746419-A-G
• gnomAD v4: 19-51746419-A-G
• MyVariant Identifiers: chr19:g.52249672A>G (hg19) ; chr19:g.51746419A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51746419A>G , CM000681.2:g.51746419A>G	GRCh38
NC_000019.9:g.52249672A>G , CM000681.1:g.52249672A>G	GRCh37
NC_000019.8:g.56941484A>G	NCBI36
NG_023426.1:g.10479T>C , LRG_146:g.10479T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000594900.2:c.576T>C	ENSP00000470750.2:p.Asn192=
ENST00000600815.2:c.576T>C	ENSP00000472936.2:p.Asn192=
ENST00000304748.5:c.576T>C MANE Select	ENSP00000302707.3:p.Asn192=
ENST00000304748.4:c.576T>C	ENSP00000302707.3:p.Asn192=
ENST00000595042.5:c.576T>C	ENSP00000471493.1:p.Asn192=
NM_001193306.1:c.576T>C	NP_001180235.1:p.Asn192=
NM_002029.3:c.576T>C , LRG_146t1:c.576T>C	NP_002020.1:p.Asn192=
NM_001193306.2:c.576T>C	NP_001180235.1:p.Asn192=
NM_002029.4:c.576T>C MANE Select	NP_002020.1:p.Asn192=