Canonical Allele Identifier: CA377619319

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601679C>A , CM000672.2:g.93601679C>A GRCh38
NC_000010.10:g.95361436C>A , CM000672.1:g.95361436C>A GRCh37
NC_000010.9:g.95351426C>A NCBI36
NG_009104.1:g.4558G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.38G>T (RBP4) ENSP00000360524.2:p.Arg13Ile
ENST00000604414.1:c.697-2395C>A (FFAR4) ENSP00000474477.1:n.697-2395C>A
ENST00000629763.2:c.38G>T (RBP4) ENSP00000487033.1:p.Arg13Ile
NM_001323518.1:c.38G>T (RBP4) NP_001310447.1:p.Arg13Ile
NM_001323518.2:c.38G>T (RBP4) NP_001310447.1:p.Arg13Ile