Canonical Allele Identifier: CA377619351

Gene: RBP4 FFAR4

Linked Data

• dbSNP Id: rs2058340734
• gnomAD v4: 10-93601686-C-T
• MyVariant Identifiers: chr10:g.95361443C>T (hg19) ; chr10:g.93601686C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93601686C>T , CM000672.2:g.93601686C>T	GRCh38
NC_000010.10:g.95361443C>T , CM000672.1:g.95361443C>T	GRCh37
NC_000010.9:g.95351433C>T	NCBI36
NG_009104.1:g.4551G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371469.2:c.31G>A (RBP4)	ENSP00000360524.2:p.Asp11Asn
ENST00000604414.1:c.697-2388C>T (FFAR4)	ENSP00000474477.1:n.697-2388C>T
ENST00000629763.2:c.31G>A (RBP4)	ENSP00000487033.1:p.Asp11Asn
NM_001323518.1:c.31G>A (RBP4)	NP_001310447.1:p.Asp11Asn
NM_001323518.2:c.31G>A (RBP4)	NP_001310447.1:p.Asp11Asn