Canonical Allele Identifier: CA407117702

Gene: FPR1

Linked Data

• dbSNP Id: rs2083744661
• MyVariant Identifiers: chr19:g.52249607A>G (hg19) ; chr19:g.51746354A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51746354A>G , CM000681.2:g.51746354A>G	GRCh38
NC_000019.9:g.52249607A>G , CM000681.1:g.52249607A>G	GRCh37
NC_000019.8:g.56941419A>G	NCBI36
NG_023426.1:g.10544T>C , LRG_146:g.10544T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594900.2:c.641T>C	ENSP00000470750.2:p.Met214Thr
ENST00000600815.2:c.641T>C	ENSP00000472936.2:p.Met214Thr
ENST00000304748.5:c.641T>C MANE Select	ENSP00000302707.3:p.Met214Thr
ENST00000304748.4:c.641T>C	ENSP00000302707.3:p.Met214Thr
ENST00000595042.5:c.641T>C	ENSP00000471493.1:p.Met214Thr
NM_001193306.1:c.641T>C	NP_001180235.1:p.Met214Thr
NM_002029.3:c.641T>C , LRG_146t1:c.641T>C	NP_002020.1:p.Met214Thr
NM_001193306.2:c.641T>C	NP_001180235.1:p.Met214Thr
NM_002029.4:c.641T>C MANE Select	NP_002020.1:p.Met214Thr