Canonical Allele Identifier: CA1928693780
Gene: RBP4 HGNC NCBI
FFAR4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601708A= , CM000672.2:g.93601708A= GRCh38
NC_000010.10:g.95361465A= , CM000672.1:g.95361465A= GRCh37
NC_000010.9:g.95351455A= NCBI36
NG_009104.1:g.4529T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371469.2:c.9T= (RBP4) ENSP00000360524.2:p.Tyr3=
ENST00000604414.1:c.697-2366A= (FFAR4) ENSP00000474477.1:n.697-2366A=
ENST00000629763.2:c.9T= (RBP4) ENSP00000487033.1:p.Tyr3=
NM_001323518.1:c.9T= (RBP4) NP_001310447.1:p.Tyr3=
NM_001323518.2:c.9T= (RBP4) NP_001310447.1:p.Tyr3=
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