Canonical Allele Identifier: CA377619308

Gene: RBP4 FFAR4

Linked Data

• dbSNP Id: rs1202659616
• gnomAD v2: 10-95361433-C-T
• gnomAD v4: 10-93601676-C-T
• MyVariant Identifiers: chr10:g.95361433C>T (hg19) ; chr10:g.93601676C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93601676C>T , CM000672.2:g.93601676C>T	GRCh38
NC_000010.10:g.95361433C>T , CM000672.1:g.95361433C>T	GRCh37
NC_000010.9:g.95351423C>T	NCBI36
NG_009104.1:g.4561G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371469.2:c.41G>A (RBP4)	ENSP00000360524.2:p.Arg14Lys
ENST00000604414.1:c.697-2398C>T (FFAR4)	ENSP00000474477.1:n.697-2398C>T
ENST00000629763.2:c.41G>A (RBP4)	ENSP00000487033.1:p.Arg14Lys
NM_001323518.1:c.41G>A (RBP4)	NP_001310447.1:p.Arg14Lys
NM_001323518.2:c.41G>A (RBP4)	NP_001310447.1:p.Arg14Lys