Canonical Allele Identifier: CA407118346

Gene: FPR1

Linked Data

• dbSNP Id: rs1293457909
• gnomAD v3: 19-51746466-T-C
• gnomAD v4: 19-51746466-T-C
• MyVariant Identifiers: chr19:g.52249719T>C (hg19) ; chr19:g.51746466T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51746466T>C , CM000681.2:g.51746466T>C	GRCh38
NC_000019.9:g.52249719T>C , CM000681.1:g.52249719T>C	GRCh37
NC_000019.8:g.56941531T>C	NCBI36
NG_023426.1:g.10432A>G , LRG_146:g.10432A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594900.2:c.529A>G	ENSP00000470750.2:p.Thr177Ala
ENST00000600815.2:c.529A>G	ENSP00000472936.2:p.Thr177Ala
ENST00000304748.5:c.529A>G MANE Select	ENSP00000302707.3:p.Thr177Ala
ENST00000304748.4:c.529A>G	ENSP00000302707.3:p.Thr177Ala
ENST00000595042.5:c.529A>G	ENSP00000471493.1:p.Thr177Ala
ENST00000600815.1:c.529A>G	ENSP00000472936.1:p.Thr177Ala
NM_001193306.1:c.529A>G	NP_001180235.1:p.Thr177Ala
NM_002029.3:c.529A>G , LRG_146t1:c.529A>G	NP_002020.1:p.Thr177Ala
NM_001193306.2:c.529A>G	NP_001180235.1:p.Thr177Ala
NM_002029.4:c.529A>G MANE Select	NP_002020.1:p.Thr177Ala