Canonical Allele Identifier: CA1928693699

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601654C= , CM000672.2:g.93601654C= GRCh38
NC_000010.10:g.95361411C= , CM000672.1:g.95361411C= GRCh37
NC_000010.9:g.95351401C= NCBI36
NG_009104.1:g.4583G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371467.5:c.-311G= (RBP4) ENSP00000360522.1:n.-311G=
ENST00000371469.2:c.51+12G= (RBP4) ENSP00000360524.2:n.51+12G=
ENST00000604414.1:c.697-2420C= (FFAR4) ENSP00000474477.1:n.697-2420C=
ENST00000629763.2:c.47+16G= (RBP4) ENSP00000487033.1:n.47+16G=
NM_001323518.1:c.51+12G= (RBP4) NP_001310447.1:n.51+12G=
NM_001323518.2:c.51+12G= (RBP4) NP_001310447.1:n.51+12G=