Canonical Allele Identifier: CA377619307

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601676C>A , CM000672.2:g.93601676C>A GRCh38
NC_000010.10:g.95361433C>A , CM000672.1:g.95361433C>A GRCh37
NC_000010.9:g.95351423C>A NCBI36
NG_009104.1:g.4561G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.41G>T (RBP4) ENSP00000360524.2:p.Arg14Met
ENST00000604414.1:c.697-2398C>A (FFAR4) ENSP00000474477.1:n.697-2398C>A
ENST00000629763.2:c.41G>T (RBP4) ENSP00000487033.1:p.Arg14Met
NM_001323518.1:c.41G>T (RBP4) NP_001310447.1:p.Arg14Met
NM_001323518.2:c.41G>T (RBP4) NP_001310447.1:p.Arg14Met