Canonical Allele Identifier: CA377619239

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601667T>C , CM000672.2:g.93601667T>C GRCh38
NC_000010.10:g.95361424T>C , CM000672.1:g.95361424T>C GRCh37
NC_000010.9:g.95351414T>C NCBI36
NG_009104.1:g.4570A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371469.2:c.50A>G (RBP4) ENSP00000360524.2:p.Glu17Gly
ENST00000604414.1:c.697-2407T>C (FFAR4) ENSP00000474477.1:n.697-2407T>C
ENST00000629763.2:c.47+3A>G (RBP4) ENSP00000487033.1:n.47+3A>G
NM_001323518.1:c.50A>G (RBP4) NP_001310447.1:p.Glu17Gly
NM_001323518.2:c.50A>G (RBP4) NP_001310447.1:p.Glu17Gly