Canonical Allele Identifier: CA2841758750
Gene: FFAR4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601754T>A , CM000672.2:g.93601754T>A GRCh38
NC_000010.10:g.95361511T>A , CM000672.1:g.95361511T>A GRCh37
NC_000010.9:g.95351501T>A NCBI36
NG_009104.1:g.4483A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000604414.1:c.697-2320T>A ENSP00000474477.1:n.697-2320T>A
Search 100 bp 5'
Search 100 bp 3'