Canonical Allele Identifier: CA5609725

Gene: RBP4 FFAR4

Linked Data

• dbSNP Id: rs750296456
• ExAC: 10:95361432 C / T
• gnomAD v2: 10-95361432-C-T
• gnomAD v3: 10-93601675-C-T
• gnomAD v4: 10-93601675-C-T
• MyVariant Identifiers: chr10:g.95361432C>T (hg19) ; chr10:g.93601675C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93601675C>T , CM000672.2:g.93601675C>T	GRCh38
NC_000010.10:g.95361432C>T , CM000672.1:g.95361432C>T	GRCh37
NC_000010.9:g.95351422C>T	NCBI36
NG_009104.1:g.4562G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371469.2:c.42G>A (RBP4)	ENSP00000360524.2:p.Arg14=
ENST00000604414.1:c.697-2399C>T (FFAR4)	ENSP00000474477.1:n.697-2399C>T
ENST00000629763.2:c.42G>A (RBP4)	ENSP00000487033.1:p.Arg14=
NM_001323518.1:c.42G>A (RBP4)	NP_001310447.1:p.Arg14=
NM_001323518.2:c.42G>A (RBP4)	NP_001310447.1:p.Arg14=