Canonical Allele Identifier: CA377619230
Gene: RBP4 HGNC NCBI
FFAR4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.95361422C>T (hg19) chr10:g.93601665C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601665C>T , CM000672.2:g.93601665C>T GRCh38
NC_000010.10:g.95361422C>T , CM000672.1:g.95361422C>T GRCh37
NC_000010.9:g.95351412C>T NCBI36
NG_009104.1:g.4572G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.51+1G>A (RBP4) ENSP00000360524.2:n.51+1G>A
ENST00000604414.1:c.697-2409C>T (FFAR4) ENSP00000474477.1:n.697-2409C>T
ENST00000629763.2:c.47+5G>A (RBP4) ENSP00000487033.1:n.47+5G>A
NM_001323518.1:c.51+1G>A (RBP4) NP_001310447.1:n.51+1G>A
NM_001323518.2:c.51+1G>A (RBP4) NP_001310447.1:n.51+1G>A
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