Canonical Allele Identifier: CA407119282
Gene: FPR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3023284
ClinVar RCV Id: RCV003882470
dbSNP Id: rs1290352179
gnomAD v2: 19-52249898-G-A
gnomAD v3: 19-51746645-G-A
gnomAD v4: 19-51746645-G-A
COSMIC: COSM6023154
MyVariant Identifiers: chr19:g.52249898G>A (hg19) chr19:g.51746645G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51746645G>A , CM000681.2:g.51746645G>A GRCh38
NC_000019.9:g.52249898G>A , CM000681.1:g.52249898G>A GRCh37
NC_000019.8:g.56941710G>A NCBI36
NG_023426.1:g.10253C>T , LRG_146:g.10253C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000594900.2:c.350C>T ENSP00000470750.2:p.Ala117Val
ENST00000600815.2:c.350C>T ENSP00000472936.2:p.Ala117Val
ENST00000304748.5:c.350C>T MANE Select ENSP00000302707.3:p.Ala117Val
ENST00000304748.4:c.350C>T ENSP00000302707.3:p.Ala117Val
ENST00000595042.5:c.350C>T ENSP00000471493.1:p.Ala117Val
ENST00000600815.1:c.350C>T ENSP00000472936.1:p.Ala117Val
NM_001193306.1:c.350C>T NP_001180235.1:p.Ala117Val
NM_002029.3:c.350C>T , LRG_146t1:c.350C>T NP_002020.1:p.Ala117Val
NM_001193306.2:c.350C>T NP_001180235.1:p.Ala117Val
NM_002029.4:c.350C>T MANE Select NP_002020.1:p.Ala117Val
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