Canonical Allele Identifier: CA2610209533
Gene: FFAR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601751T>C , CM000672.2:g.93601751T>C GRCh38
NC_000010.10:g.95361508T>C , CM000672.1:g.95361508T>C GRCh37
NC_000010.9:g.95351498T>C NCBI36
NG_009104.1:g.4486A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000604414.1:c.697-2323T>C ENSP00000474477.1:n.697-2323T>C