Canonical Allele Identifier: CA5609722

Gene: RBP4 FFAR4

Linked Data

• dbSNP Id: rs542970357
• ExAC: 10:95361426 C / A
• gnomAD v2: 10-95361426-C-A
• gnomAD v4: 10-93601669-C-A
• MyVariant Identifiers: chr10:g.95361426C>A (hg19) ; chr10:g.93601669C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93601669C>A , CM000672.2:g.93601669C>A	GRCh38
NC_000010.10:g.95361426C>A , CM000672.1:g.95361426C>A	GRCh37
NC_000010.9:g.95351416C>A	NCBI36
NG_009104.1:g.4568G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371469.2:c.48G>T (RBP4)	ENSP00000360524.2:p.Thr16=
ENST00000604414.1:c.697-2405C>A (FFAR4)	ENSP00000474477.1:n.697-2405C>A
ENST00000629763.2:c.47+1G>T (RBP4)	ENSP00000487033.1:n.47+1G>T
NM_001323518.1:c.48G>T (RBP4)	NP_001310447.1:p.Thr16=
NM_001323518.2:c.48G>T (RBP4)	NP_001310447.1:p.Thr16=