Canonical Allele Identifier: CA1928693713

Linked Data

dbSNP Id: rs2058340553

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601672C>T , CM000672.2:g.93601672C>T GRCh38
NC_000010.10:g.95361429C>T , CM000672.1:g.95361429C>T GRCh37
NC_000010.9:g.95351419C>T NCBI36
NG_009104.1:g.4565G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371469.2:c.45G>A (RBP4) ENSP00000360524.2:p.Gln15=
ENST00000604414.1:c.697-2402C>T (FFAR4) ENSP00000474477.1:n.697-2402C>T
ENST00000629763.2:c.45G>A (RBP4) ENSP00000487033.1:p.Gln15=
NM_001323518.1:c.45G>A (RBP4) NP_001310447.1:p.Gln15=
NM_001323518.2:c.45G>A (RBP4) NP_001310447.1:p.Gln15=