Canonical Allele Identifier: CA1928693851
Gene: FFAR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601756T= , CM000672.2:g.93601756T= GRCh38
NC_000010.10:g.95361513T= , CM000672.1:g.95361513T= GRCh37
NC_000010.9:g.95351503T= NCBI36
NG_009104.1:g.4481A=

Transcript Alleles

HGVS Amino-acid change
ENST00000604414.1:c.697-2318T= ENSP00000474477.1:n.697-2318T=