Canonical Allele Identifier: CA2610209435

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601585C>A , CM000672.2:g.93601585C>A GRCh38
NC_000010.10:g.95361342C>A , CM000672.1:g.95361342C>A GRCh37
NC_000010.9:g.95351332C>A NCBI36
NG_009104.1:g.4652G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371467.5:c.-242G>T (RBP4) ENSP00000360522.1:n.-242G>T
ENST00000371469.2:c.51+81G>T (RBP4) ENSP00000360524.2:n.51+81G>T
ENST00000604414.1:c.697-2489C>A (FFAR4) ENSP00000474477.1:n.697-2489C>A
ENST00000629763.2:c.47+85G>T (RBP4) ENSP00000487033.1:n.47+85G>T
NM_001323518.1:c.51+81G>T (RBP4) NP_001310447.1:n.51+81G>T
NM_001323518.2:c.51+81G>T (RBP4) NP_001310447.1:n.51+81G>T