Canonical Allele Identifier: CA343184978

Gene: FMO2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171207773T>A , CM000663.2:g.171207773T>A	GRCh38
NC_000001.10:g.171176912T>A , CM000663.1:g.171176912T>A	GRCh37
NC_000001.9:g.169443536T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209929.10:c.1239T>A MANE Select	ENSP00000209929.8:p.Asn413Lys
ENST00000209929.9:c.1239T>A	ENSP00000209929.8:p.Asn413Lys
ENST00000488431.1:n.231T>A
ENST00000529935.5:c.1024T>A	ENSP00000487002.1:n.1024T>A
NM_001301347.1:c.579T>A	NP_001288276.1:p.Asn193Lys
NM_001460.4:c.1239T>A	NP_001451.2:p.Asn413Lys
XR_426768.2:n.1356T>A
XR_921761.1:n.1356T>A
XR_922278.1:n.508-39585A>T
NM_001365900.1:c.1044T>A	NP_001352829.1:p.Asn348Lys
NR_158622.1:n.1259T>A
XR_001737072.2:n.1306T>A
XR_001738291.2:n.1307-39585A>T
XR_921761.3:n.1306T>A
XR_922278.3:n.1307-39585A>T
NM_001460.5:c.1239T>A MANE Select	NP_001451.2:p.Asn413Lys
NR_160266.1:n.1167T>A
NM_001301347.2:c.579T>A	NP_001288276.1:p.Asn193Lys