Canonical Allele Identifier: CA309808508

Gene: FPR1

Linked Data

• ClinVar Variation Id: 3007275
• ClinVar RCV Id: RCV003868914
• dbSNP Id: rs752024794
• gnomAD v2: 19-52249843-G-A
• gnomAD v4: 19-51746590-G-A
• MyVariant Identifiers: chr19:g.52249843G>A (hg19) ; chr19:g.51746590G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51746590G>A , CM000681.2:g.51746590G>A	GRCh38
NC_000019.9:g.52249843G>A , CM000681.1:g.52249843G>A	GRCh37
NC_000019.8:g.56941655G>A	NCBI36
NG_023426.1:g.10308C>T , LRG_146:g.10308C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594900.2:c.405C>T	ENSP00000470750.2:p.Asn135=
ENST00000600815.2:c.405C>T	ENSP00000472936.2:p.Asn135=
ENST00000304748.5:c.405C>T MANE Select	ENSP00000302707.3:p.Asn135=
ENST00000304748.4:c.405C>T	ENSP00000302707.3:p.Asn135=
ENST00000595042.5:c.405C>T	ENSP00000471493.1:p.Asn135=
ENST00000600815.1:c.405C>T	ENSP00000472936.1:p.Asn135=
NM_001193306.1:c.405C>T	NP_001180235.1:p.Asn135=
NM_002029.3:c.405C>T , LRG_146t1:c.405C>T	NP_002020.1:p.Asn135=
NM_001193306.2:c.405C>T	NP_001180235.1:p.Asn135=
NM_002029.4:c.405C>T MANE Select	NP_002020.1:p.Asn135=