Canonical Allele Identifier: CA2610209492

Linked Data

Genomic Alleles

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

Transcript Alleles

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