Canonical Allele Identifier: CA595272798

Gene: RBP4 FFAR4

Linked Data

• dbSNP Id: rs1443418942
• gnomAD v2: 10-95361385-G-A
• gnomAD v3: 10-93601628-G-A
• gnomAD v4: 10-93601628-G-A
• MyVariant Identifiers: chr10:g.95361385G>A (hg19) ; chr10:g.93601628G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93601628G>A , CM000672.2:g.93601628G>A	GRCh38
NC_000010.10:g.95361385G>A , CM000672.1:g.95361385G>A	GRCh37
NC_000010.9:g.95351375G>A	NCBI36
NG_009104.1:g.4609C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371467.5:c.-285C>T (RBP4)	ENSP00000360522.1:n.-285C>T
ENST00000371469.2:c.51+38C>T (RBP4)	ENSP00000360524.2:n.51+38C>T
ENST00000604414.1:c.697-2446G>A (FFAR4)	ENSP00000474477.1:n.697-2446G>A
ENST00000629763.2:c.47+42C>T (RBP4)	ENSP00000487033.1:n.47+42C>T
NM_001323518.1:c.51+38C>T (RBP4)	NP_001310447.1:n.51+38C>T
NM_001323518.2:c.51+38C>T (RBP4)	NP_001310447.1:n.51+38C>T