Canonical Allele Identifier: CA377619380

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601694G>C , CM000672.2:g.93601694G>C GRCh38
NC_000010.10:g.95361451G>C , CM000672.1:g.95361451G>C GRCh37
NC_000010.9:g.95351441G>C NCBI36
NG_009104.1:g.4543C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371469.2:c.23C>G (RBP4) ENSP00000360524.2:p.Ala8Gly
ENST00000604414.1:c.697-2380G>C (FFAR4) ENSP00000474477.1:n.697-2380G>C
ENST00000629763.2:c.23C>G (RBP4) ENSP00000487033.1:p.Ala8Gly
NM_001323518.1:c.23C>G (RBP4) NP_001310447.1:p.Ala8Gly
NM_001323518.2:c.23C>G (RBP4) NP_001310447.1:p.Ala8Gly