Canonical Allele Identifier: CA377619384

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601695C>A , CM000672.2:g.93601695C>A GRCh38
NC_000010.10:g.95361452C>A , CM000672.1:g.95361452C>A GRCh37
NC_000010.9:g.95351442C>A NCBI36
NG_009104.1:g.4542G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371469.2:c.22G>T (RBP4) ENSP00000360524.2:p.Ala8Ser
ENST00000604414.1:c.697-2379C>A (FFAR4) ENSP00000474477.1:n.697-2379C>A
ENST00000629763.2:c.22G>T (RBP4) ENSP00000487033.1:p.Ala8Ser
NM_001323518.1:c.22G>T (RBP4) NP_001310447.1:p.Ala8Ser
NM_001323518.2:c.22G>T (RBP4) NP_001310447.1:p.Ala8Ser