Canonical Allele Identifier: CA377619250

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601668C>G , CM000672.2:g.93601668C>G GRCh38
NC_000010.10:g.95361425C>G , CM000672.1:g.95361425C>G GRCh37
NC_000010.9:g.95351415C>G NCBI36
NG_009104.1:g.4569G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.49G>C (RBP4) ENSP00000360524.2:p.Glu17Gln
ENST00000604414.1:c.697-2406C>G (FFAR4) ENSP00000474477.1:n.697-2406C>G
ENST00000629763.2:c.47+2G>C (RBP4) ENSP00000487033.1:n.47+2G>C
NM_001323518.1:c.49G>C (RBP4) NP_001310447.1:p.Glu17Gln
NM_001323518.2:c.49G>C (RBP4) NP_001310447.1:p.Glu17Gln