Canonical Allele Identifier: CA211559395

Linked Data

dbSNP Id: rs935072996

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601741G>A , CM000672.2:g.93601741G>A GRCh38
NC_000010.10:g.95361498G>A , CM000672.1:g.95361498G>A GRCh37
NC_000010.9:g.95351488G>A NCBI36
NG_009104.1:g.4496C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.-25C>T (RBP4) ENSP00000360524.2:n.-25C>T
ENST00000604414.1:c.697-2333G>A (FFAR4) ENSP00000474477.1:n.697-2333G>A
NM_001323518.1:c.-25C>T (RBP4) NP_001310447.1:n.-25C>T
NM_001323518.2:c.-25C>T (RBP4) NP_001310447.1:n.-25C>T