Canonical Allele Identifier: CA1928693711

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601672C= , CM000672.2:g.93601672C= GRCh38
NC_000010.10:g.95361429C= , CM000672.1:g.95361429C= GRCh37
NC_000010.9:g.95351419C= NCBI36
NG_009104.1:g.4565G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.45G= (RBP4) ENSP00000360524.2:p.Gln15=
ENST00000604414.1:c.697-2402C= (FFAR4) ENSP00000474477.1:n.697-2402C=
ENST00000629763.2:c.45G= (RBP4) ENSP00000487033.1:p.Gln15=
NM_001323518.1:c.45G= (RBP4) NP_001310447.1:p.Gln15=
NM_001323518.2:c.45G= (RBP4) NP_001310447.1:p.Gln15=