Canonical Allele Identifier: CA377619313

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601677T>C , CM000672.2:g.93601677T>C GRCh38
NC_000010.10:g.95361434T>C , CM000672.1:g.95361434T>C GRCh37
NC_000010.9:g.95351424T>C NCBI36
NG_009104.1:g.4560A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.40A>G (RBP4) ENSP00000360524.2:p.Arg14Gly
ENST00000604414.1:c.697-2397T>C (FFAR4) ENSP00000474477.1:n.697-2397T>C
ENST00000629763.2:c.40A>G (RBP4) ENSP00000487033.1:p.Arg14Gly
NM_001323518.1:c.40A>G (RBP4) NP_001310447.1:p.Arg14Gly
NM_001323518.2:c.40A>G (RBP4) NP_001310447.1:p.Arg14Gly