Canonical Allele Identifier: CA1139908968

Gene: FMO2

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_001460.5:c.1239T= MANE Select	NP_001451.2:p.Asn413=
ENST00000209929.10:c.1239T= MANE Select	ENSP00000209929.8:p.Asn413=
NM_001301347.1:c.579T=	NP_001288276.1:p.Asn193=
NM_001301347.2:c.579T=	NP_001288276.1:p.Asn193=
NM_001365900.1:c.1044T=	NP_001352829.1:p.Asn348=
NM_001460.4:c.1239T=	NP_001451.2:p.Asn413=
NR_158622.1:n.1259T=
NR_160266.1:n.1167T=
ENST00000209929.9:c.1239T=	ENSP00000209929.8:p.Asn413=
ENST00000488431.1:n.231T=
ENST00000529935.5:c.1024T=	ENSP00000487002.1:n.1024T=
XR_001737072.2:n.1306T=
XR_001738291.2:n.1307-39585A=
XR_426768.2:n.1356T=
XR_921761.1:n.1356T=
XR_921761.3:n.1306T=
XR_922278.1:n.508-39585A=
XR_922278.3:n.1307-39585A=