Canonical Allele Identifier: CA129457

Gene: FFAR4

Linked Data

• ClinVar Variation Id: 30774
• ClinVar RCV Id: RCV000023753
• dbSNP Id: rs116454156
• ExAC: 10:95347041 G / A
• gnomAD v2: 10-95347041-G-A
• gnomAD v3: 10-93587284-G-A
• gnomAD v4: 10-93587284-G-A
• MyVariant Identifiers: chr10:g.95347041G>A (hg19) ; chr10:g.93587284G>A (hg38)
• PubMed: PMID:22343897 ; PMID:27068006

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93587284G>A , CM000672.2:g.93587284G>A	GRCh38
NC_000010.10:g.95347041G>A , CM000672.1:g.95347041G>A	GRCh37
NC_000010.9:g.95337031G>A	NCBI36
NG_032670.1:g.25620G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371481.9:c.761G>A MANE Select	ENSP00000360536.5:p.Arg254His
ENST00000371481.8:c.761G>A	ENSP00000360536.4:p.Arg254His
ENST00000371483.8:c.809G>A	ENSP00000360538.4:p.Arg270His
ENST00000604414.1:c.696+11065G>A	ENSP00000474477.1:n.696+11065G>A
NM_001195755.1:c.761G>A	NP_001182684.1:p.Arg254His
NM_181745.3:c.809G>A	NP_859529.2:p.Arg270His
NM_001195755.2:c.761G>A MANE Select	NP_001182684.1:p.Arg254His
NM_181745.4:c.809G>A	NP_859529.2:p.Arg270His