Canonical Allele Identifier: CA1928693792

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601717C= , CM000672.2:g.93601717C= GRCh38
NC_000010.10:g.95361474C= , CM000672.1:g.95361474C= GRCh37
NC_000010.9:g.95351464C= NCBI36
NG_009104.1:g.4520G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371469.2:c.-1G= (RBP4) ENSP00000360524.2:n.-1G=
ENST00000604414.1:c.697-2357C= (FFAR4) ENSP00000474477.1:n.697-2357C=
NM_001323518.1:c.-1G= (RBP4) NP_001310447.1:n.-1G=
NM_001323518.2:c.-1G= (RBP4) NP_001310447.1:n.-1G=