Canonical Allele Identifier: CA9616408

Gene: FPR1

Linked Data

• ClinVar Variation Id: 1986440
• ClinVar RCV Id: RCV002786194
• dbSNP Id: rs775825440
• ExAC: 19:52249600 G / A
• gnomAD v2: 19-52249600-G-A
• gnomAD v3: 19-51746347-G-A
• gnomAD v4: 19-51746347-G-A
• COSMIC: COSM3537882
• MyVariant Identifiers: chr19:g.52249600G>A (hg19) ; chr19:g.51746347G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51746347G>A , CM000681.2:g.51746347G>A	GRCh38
NC_000019.9:g.52249600G>A , CM000681.1:g.52249600G>A	GRCh37
NC_000019.8:g.56941412G>A	NCBI36
NG_023426.1:g.10551C>T , LRG_146:g.10551C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594900.2:c.648C>T	ENSP00000470750.2:p.Ile216=
ENST00000600815.2:c.648C>T	ENSP00000472936.2:p.Ile216=
ENST00000304748.5:c.648C>T MANE Select	ENSP00000302707.3:p.Ile216=
ENST00000304748.4:c.648C>T	ENSP00000302707.3:p.Ile216=
ENST00000595042.5:c.648C>T	ENSP00000471493.1:p.Ile216=
NM_001193306.1:c.648C>T	NP_001180235.1:p.Ile216=
NM_002029.3:c.648C>T , LRG_146t1:c.648C>T	NP_002020.1:p.Ile216=
NM_001193306.2:c.648C>T	NP_001180235.1:p.Ile216=
NM_002029.4:c.648C>T MANE Select	NP_002020.1:p.Ile216=