Canonical Allele Identifier: CA670065394
Gene: RBP4 HGNC NCBI
FFAR4 HGNC NCBI

Linked Data

dbSNP Id: rs1490289387
gnomAD v3: 10-93601729-T-G
gnomAD v4: 10-93601729-T-G
MyVariant Identifiers: chr10:g.95361486T>G (hg19) chr10:g.93601729T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601729T>G , CM000672.2:g.93601729T>G GRCh38
NC_000010.10:g.95361486T>G , CM000672.1:g.95361486T>G GRCh37
NC_000010.9:g.95351476T>G NCBI36
NG_009104.1:g.4508A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371469.2:c.-13A>C (RBP4) ENSP00000360524.2:n.-13A>C
ENST00000604414.1:c.697-2345T>G (FFAR4) ENSP00000474477.1:n.697-2345T>G
NM_001323518.1:c.-13A>C (RBP4) NP_001310447.1:n.-13A>C
NM_001323518.2:c.-13A>C (RBP4) NP_001310447.1:n.-13A>C
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