Canonical Allele Identifier: CA1928693913
Community Standard Title: NC_000010.11:g.93601831C=
Gene: FFAR4 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000604414.1:c.697-2243C= ENSP00000474477.1:n.697-2243C=