Canonical Allele Identifier: CA211559399

Gene: RBP4 FFAR4

Linked Data

• dbSNP Id: rs991960445
• gnomAD v2: 10-95361501-T-C
• gnomAD v4: 10-93601744-T-C
• MyVariant Identifiers: chr10:g.95361501T>C (hg19) ; chr10:g.93601744T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93601744T>C , CM000672.2:g.93601744T>C	GRCh38
NC_000010.10:g.95361501T>C , CM000672.1:g.95361501T>C	GRCh37
NC_000010.9:g.95351491T>C	NCBI36
NG_009104.1:g.4493A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371469.2:c.-28A>G (RBP4)	ENSP00000360524.2:n.-28A>G
ENST00000604414.1:c.697-2330T>C (FFAR4)	ENSP00000474477.1:n.697-2330T>C
NM_001323518.1:c.-28A>G (RBP4)	NP_001310447.1:n.-28A>G
NM_001323518.2:c.-28A>G (RBP4)	NP_001310447.1:n.-28A>G