Canonical Allele Identifier: CA595272792

Gene: RBP4 FFAR4

Linked Data

• dbSNP Id: rs1273913948
• gnomAD v2: 10-95361372-G-C
• gnomAD v3: 10-93601615-G-C
• gnomAD v4: 10-93601615-G-C
• MyVariant Identifiers: chr10:g.95361372G>C (hg19) ; chr10:g.93601615G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93601615G>C , CM000672.2:g.93601615G>C	GRCh38
NC_000010.10:g.95361372G>C , CM000672.1:g.95361372G>C	GRCh37
NC_000010.9:g.95351362G>C	NCBI36
NG_009104.1:g.4622C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371467.5:c.-272C>G (RBP4)	ENSP00000360522.1:n.-272C>G
ENST00000371469.2:c.51+51C>G (RBP4)	ENSP00000360524.2:n.51+51C>G
ENST00000604414.1:c.697-2459G>C (FFAR4)	ENSP00000474477.1:n.697-2459G>C
ENST00000629763.2:c.47+55C>G (RBP4)	ENSP00000487033.1:n.47+55C>G
NM_001323518.1:c.51+51C>G (RBP4)	NP_001310447.1:n.51+51C>G
NM_001323518.2:c.51+51C>G (RBP4)	NP_001310447.1:n.51+51C>G