Canonical Allele Identifier: CA211559397

Linked Data

dbSNP Id: rs901259584

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601743A>T , CM000672.2:g.93601743A>T GRCh38
NC_000010.10:g.95361500A>T , CM000672.1:g.95361500A>T GRCh37
NC_000010.9:g.95351490A>T NCBI36
NG_009104.1:g.4494T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.-27T>A (RBP4) ENSP00000360524.2:n.-27T>A
ENST00000604414.1:c.697-2331A>T (FFAR4) ENSP00000474477.1:n.697-2331A>T
NM_001323518.1:c.-27T>A (RBP4) NP_001310447.1:n.-27T>A
NM_001323518.2:c.-27T>A (RBP4) NP_001310447.1:n.-27T>A