Canonical Allele Identifier: CA1928693790

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601715A= , CM000672.2:g.93601715A= GRCh38
NC_000010.10:g.95361472A= , CM000672.1:g.95361472A= GRCh37
NC_000010.9:g.95351462A= NCBI36
NG_009104.1:g.4522T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371469.2:c.2T= (RBP4) ENSP00000360524.2:p.Met1=
ENST00000604414.1:c.697-2359A= (FFAR4) ENSP00000474477.1:n.697-2359A=
ENST00000629763.2:c.2T= (RBP4) ENSP00000487033.1:p.Met1=
NM_001323518.1:c.2T= (RBP4) NP_001310447.1:p.Met1=
NM_001323518.2:c.2T= (RBP4) NP_001310447.1:p.Met1=