Canonical Allele Identifier: CA5609576
Gene: RBP4 HGNC NCBI
FFAR4 HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.93594060C>G
GRCh37 chr10:g.95353817C>G
gnomAD v2:
10:95353817 C / G
gnomAD v3:
10:93594060 C / G
gnomAD v4:
chr10-93594060-C-G
Joint Max Group AF 0.34357903 (AFR)
Genomes Max Group AF 0.33713051 (AFR)
Exomes Max Group AF 0.34832631 (AFR)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93594060C>G , CM000672.2:g.93594060C>G GRCh38
NC_000010.10:g.95353817C>G , CM000672.1:g.95353817C>G GRCh37
NC_000010.9:g.95343807C>G NCBI36
NG_009104.1:g.12177G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371464.8:c.356-25G>C (RBP4) MANE Select ENSP00000360519.3:n.356-25G>C
ENST00000371464.7:c.356-25G>C (RBP4) ENSP00000360519.3:n.356-25G>C
ENST00000371467.5:c.356-25G>C (RBP4) ENSP00000360522.1:n.356-25G>C
ENST00000371469.2:c.350-25G>C (RBP4) ENSP00000360524.2:n.350-25G>C
ENST00000604414.1:c.697-10014C>G (FFAR4) ENSP00000474477.1:n.697-10014C>G
ENST00000615669.4:c.350-25G>C (RBP4) ENSP00000480654.1:n.350-25G>C
ENST00000629763.2:c.350-25G>C (RBP4) ENSP00000487033.1:n.350-25G>C
NM_006744.3:c.356-25G>C (RBP4) NP_006735.2:n.356-25G>C
NM_001323517.1:c.356-25G>C (RBP4) NP_001310446.1:n.356-25G>C
NM_001323518.1:c.350-25G>C (RBP4) NP_001310447.1:n.350-25G>C
NM_006744.4:c.356-25G>C (RBP4) MANE Select NP_006735.2:n.356-25G>C
NM_001323518.2:c.350-25G>C (RBP4) NP_001310447.1:n.350-25G>C
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