Canonical Allele Identifier: CA5609737

Gene: FFAR4

Linked Data

• dbSNP Id: rs773419725
• ExAC: 10:95361512 CTCTT / C
• gnomAD v2: 10-95361512-CTCTT-C
• gnomAD v3: 10-93601755-CTCTT-C
• gnomAD v4: 10-93601755-CTCTT-C
• MyVariant Identifiers: chr10:g.95361513_95361516del (hg19) ; chr10:g.93601757_93601760del (hg38) ; chr10:g.93601756_93601759del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93601758_93601761del , CM000672.2:g.93601758_93601761del	GRCh38
NC_000010.10:g.95361515_95361518del , CM000672.1:g.95361515_95361518del	GRCh37
NC_000010.9:g.95351505_95351508del	NCBI36
NG_009104.1:g.4478_4481del

Transcript Alleles

HGVS	Amino-acid change
ENST00000604414.1:c.697-2316_697-2313del	ENSP00000474477.1:n.697-2316_697-2313del