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Canonical Allele Identifier:
CA377619384
Gene: RBP4
HGNC
NCBI
FFAR4
HGNC
NCBI
Linked Data
gnomAD v4:
10-93601695-C-A
MyVariant Identifiers:
chr10:g.95361452C>A (hg19)
chr10:g.93601695C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.93601695C>A , CM000672.2:g.93601695C>A
GRCh38
NC_000010.10:g.95361452C>A , CM000672.1:g.95361452C>A
GRCh37
NC_000010.9:g.95351442C>A
NCBI36
NG_009104.1:g.4542G>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000371469.2:c.22G>T
(RBP4)
ENSP00000360524.2:p.Ala8Ser
ENST00000604414.1:c.697-2379C>A
(FFAR4)
ENSP00000474477.1:n.697-2379C>A
ENST00000629763.2:c.22G>T
(RBP4)
ENSP00000487033.1:p.Ala8Ser
NM_001323518.1:c.22G>T
(RBP4)
NP_001310447.1:p.Ala8Ser
NM_001323518.2:c.22G>T
(RBP4)
NP_001310447.1:p.Ala8Ser
Search 100 bp 5'
Search 100 bp 3'