Canonical Allele Identifier: CA670065238
Gene: RBP4 HGNC NCBI
FFAR4 HGNC NCBI

Linked Data

dbSNP Id: rs1215726290
gnomAD v3: 10-93601570-A-G
gnomAD v4: 10-93601570-A-G
MyVariant Identifiers: chr10:g.95361327A>G (hg19) chr10:g.93601570A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601570A>G , CM000672.2:g.93601570A>G GRCh38
NC_000010.10:g.95361327A>G , CM000672.1:g.95361327A>G GRCh37
NC_000010.9:g.95351317A>G NCBI36
NG_009104.1:g.4667T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371467.5:c.-227T>C (RBP4) ENSP00000360522.1:n.-227T>C
ENST00000371469.2:c.51+96T>C (RBP4) ENSP00000360524.2:n.51+96T>C
ENST00000604414.1:c.697-2504A>G (FFAR4) ENSP00000474477.1:n.697-2504A>G
ENST00000629763.2:c.47+100T>C (RBP4) ENSP00000487033.1:n.47+100T>C
NM_001323518.1:c.51+96T>C (RBP4) NP_001310447.1:n.51+96T>C
NM_001323518.2:c.51+96T>C (RBP4) NP_001310447.1:n.51+96T>C
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