Canonical Allele Identifier: CA595272818

Gene: RBP4 FFAR4

Linked Data

• dbSNP Id: rs1383201897
• gnomAD v2: 10-95361413-A-G
• gnomAD v4: 10-93601656-A-G
• MyVariant Identifiers: chr10:g.95361413A>G (hg19) ; chr10:g.93601656A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93601656A>G , CM000672.2:g.93601656A>G	GRCh38
NC_000010.10:g.95361413A>G , CM000672.1:g.95361413A>G	GRCh37
NC_000010.9:g.95351403A>G	NCBI36
NG_009104.1:g.4581T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371467.5:c.-313T>C (RBP4)	ENSP00000360522.1:n.-313T>C
ENST00000371469.2:c.51+10T>C (RBP4)	ENSP00000360524.2:n.51+10T>C
ENST00000604414.1:c.697-2418A>G (FFAR4)	ENSP00000474477.1:n.697-2418A>G
ENST00000629763.2:c.47+14T>C (RBP4)	ENSP00000487033.1:n.47+14T>C
NM_001323518.1:c.51+10T>C (RBP4)	NP_001310447.1:n.51+10T>C
NM_001323518.2:c.51+10T>C (RBP4)	NP_001310447.1:n.51+10T>C