Canonical Allele Identifier: CA5609720

Linked Data

dbSNP Id: rs574006118

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601658A>G , CM000672.2:g.93601658A>G GRCh38
NC_000010.10:g.95361415A>G , CM000672.1:g.95361415A>G GRCh37
NC_000010.9:g.95351405A>G NCBI36
NG_009104.1:g.4579T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371467.5:c.-315T>C (RBP4) ENSP00000360522.1:n.-315T>C
ENST00000371469.2:c.51+8T>C (RBP4) ENSP00000360524.2:n.51+8T>C
ENST00000604414.1:c.697-2416A>G (FFAR4) ENSP00000474477.1:n.697-2416A>G
ENST00000629763.2:c.47+12T>C (RBP4) ENSP00000487033.1:n.47+12T>C
NM_001323518.1:c.51+8T>C (RBP4) NP_001310447.1:n.51+8T>C
NM_001323518.2:c.51+8T>C (RBP4) NP_001310447.1:n.51+8T>C