Canonical Allele Identifier: CA2610209534
Gene: FFAR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601752A>G , CM000672.2:g.93601752A>G GRCh38
NC_000010.10:g.95361509A>G , CM000672.1:g.95361509A>G GRCh37
NC_000010.9:g.95351499A>G NCBI36
NG_009104.1:g.4485T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000604414.1:c.697-2322A>G ENSP00000474477.1:n.697-2322A>G