Canonical Allele Identifier: CA309808142

Gene: FPR1

Linked Data

• dbSNP Id: rs991593657
• MyVariant Identifiers: chr19:g.52249623C>T (hg19) ; chr19:g.51746370C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51746370C>T , CM000681.2:g.51746370C>T	GRCh38
NC_000019.9:g.52249623C>T , CM000681.1:g.52249623C>T	GRCh37
NC_000019.8:g.56941435C>T	NCBI36
NG_023426.1:g.10528G>A , LRG_146:g.10528G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594900.2:c.625G>A	ENSP00000470750.2:p.Gly209Ser
ENST00000600815.2:c.625G>A	ENSP00000472936.2:p.Gly209Ser
ENST00000304748.5:c.625G>A MANE Select	ENSP00000302707.3:p.Gly209Ser
ENST00000304748.4:c.625G>A	ENSP00000302707.3:p.Gly209Ser
ENST00000595042.5:c.625G>A	ENSP00000471493.1:p.Gly209Ser
NM_001193306.1:c.625G>A	NP_001180235.1:p.Gly209Ser
NM_002029.3:c.625G>A , LRG_146t1:c.625G>A	NP_002020.1:p.Gly209Ser
NM_001193306.2:c.625G>A	NP_001180235.1:p.Gly209Ser
NM_002029.4:c.625G>A MANE Select	NP_002020.1:p.Gly209Ser