Canonical Allele Identifier: CA377619278

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601671T>C , CM000672.2:g.93601671T>C GRCh38
NC_000010.10:g.95361428T>C , CM000672.1:g.95361428T>C GRCh37
NC_000010.9:g.95351418T>C NCBI36
NG_009104.1:g.4566A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.46A>G (RBP4) ENSP00000360524.2:p.Thr16Ala
ENST00000604414.1:c.697-2403T>C (FFAR4) ENSP00000474477.1:n.697-2403T>C
ENST00000629763.2:c.46A>G (RBP4) ENSP00000487033.1:p.Thr16Ala
NM_001323518.1:c.46A>G (RBP4) NP_001310447.1:p.Thr16Ala
NM_001323518.2:c.46A>G (RBP4) NP_001310447.1:p.Thr16Ala