Canonical Allele Identifier: CA9378204

Gene: FFAR2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35450366C>T , CM000681.2:g.35450366C>T	GRCh38
NC_000019.9:g.35941268C>T , CM000681.1:g.35941268C>T	GRCh37
NC_000019.8:g.40633108C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001370087.1:c.652C>T MANE Select	NP_001357016.1:p.Arg218Cys
ENST00000599180.3:c.652C>T MANE Select	ENSP00000473159.1:p.Arg218Cys
NM_005306.2:c.652C>T	NP_005297.1:p.Arg218Cys
NM_005306.3:c.652C>T	NP_005297.1:p.Arg218Cys
ENST00000246549.2:c.652C>T	ENSP00000246549.2:p.Arg218Cys
ENST00000599180.2:c.652C>T	ENSP00000473159.1:p.Arg218Cys
ENST00000601590.1:n.17-787C>T
XM_017026709.1:c.652C>T	XP_016882198.1:p.Arg218Cys
XM_017026710.2:c.652C>T	XP_016882199.1:p.Arg218Cys
XM_017026711.1:c.652C>T	XP_016882200.1:p.Arg218Cys