Canonical Allele Identifier: CA1928693835

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601744T= , CM000672.2:g.93601744T= GRCh38
NC_000010.10:g.95361501T= , CM000672.1:g.95361501T= GRCh37
NC_000010.9:g.95351491T= NCBI36
NG_009104.1:g.4493A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.-28A= (RBP4) ENSP00000360524.2:n.-28A=
ENST00000604414.1:c.697-2330T= (FFAR4) ENSP00000474477.1:n.697-2330T=
NM_001323518.1:c.-28A= (RBP4) NP_001310447.1:n.-28A=
NM_001323518.2:c.-28A= (RBP4) NP_001310447.1:n.-28A=