Canonical Allele Identifier: CA595272820

Linked Data

dbSNP Id: rs1312755502

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601662G>T , CM000672.2:g.93601662G>T GRCh38
NC_000010.10:g.95361419G>T , CM000672.1:g.95361419G>T GRCh37
NC_000010.9:g.95351409G>T NCBI36
NG_009104.1:g.4575C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371467.5:c.-319C>A (RBP4) ENSP00000360522.1:n.-319C>A
ENST00000371469.2:c.51+4C>A (RBP4) ENSP00000360524.2:n.51+4C>A
ENST00000604414.1:c.697-2412G>T (FFAR4) ENSP00000474477.1:n.697-2412G>T
ENST00000629763.2:c.47+8C>A (RBP4) ENSP00000487033.1:n.47+8C>A
NM_001323518.1:c.51+4C>A (RBP4) NP_001310447.1:n.51+4C>A
NM_001323518.2:c.51+4C>A (RBP4) NP_001310447.1:n.51+4C>A