Canonical Allele Identifier: CA931297446

Gene: FFAR4

Linked Data

• dbSNP Id: rs2058341405
• gnomAD v3: 10-93601757-C-CT
• gnomAD v4: 10-93601757-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93601760dup , CM000672.2:g.93601760dup	GRCh38
NC_000010.10:g.95361517dup , CM000672.1:g.95361517dup	GRCh37
NC_000010.9:g.95351507dup	NCBI36
NG_009104.1:g.4479dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000604414.1:c.697-2314dup	ENSP00000474477.1:n.697-2314dup