Canonical Allele Identifier: CA1928693841
Gene: FFAR4 HGNC NCBI

Linked Data

dbSNP Id: rs2058341281

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601746T>C , CM000672.2:g.93601746T>C GRCh38
NC_000010.10:g.95361503T>C , CM000672.1:g.95361503T>C GRCh37
NC_000010.9:g.95351493T>C NCBI36
NG_009104.1:g.4491A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000604414.1:c.697-2328T>C ENSP00000474477.1:n.697-2328T>C