Canonical Allele Identifier: CA211559426

Gene: FFAR4

Linked Data

• dbSNP Id: rs993966503
• gnomAD v2: 10-95361519-A-G
• gnomAD v4: 10-93601762-A-G
• MyVariant Identifiers: chr10:g.95361519A>G (hg19) ; chr10:g.93601762A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93601762A>G , CM000672.2:g.93601762A>G	GRCh38
NC_000010.10:g.95361519A>G , CM000672.1:g.95361519A>G	GRCh37
NC_000010.9:g.95351509A>G	NCBI36
NG_009104.1:g.4475T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000604414.1:c.697-2312A>G	ENSP00000474477.1:n.697-2312A>G