Canonical Allele Identifier: CA13165082
Gene: FFAR4 HGNC NCBI

Linked Data

dbSNP Id: rs3758539

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601831C>T , CM000672.2:g.93601831C>T GRCh38
NC_000010.10:g.95361588C>T , CM000672.1:g.95361588C>T GRCh37
NC_000010.9:g.95351578C>T NCBI36
NG_009104.1:g.4406G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000604414.1:c.697-2243C>T ENSP00000474477.1:n.697-2243C>T