Canonical Allele Identifier: CA2722560959
Gene: FFAR4 HGNC NCBI

Linked Data

dbSNP Id: rs2134577805

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601751del , CM000672.2:g.93601751del GRCh38
NC_000010.10:g.95361508del , CM000672.1:g.95361508del GRCh37
NC_000010.9:g.95351498del NCBI36
NG_009104.1:g.4489del

Transcript Alleles

HGVS Amino-acid change
ENST00000604414.1:c.697-2323del ENSP00000474477.1:n.697-2323del