Canonical Allele Identifier: CA1139908964

Gene: FMO2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171199445C= , CM000663.2:g.171199445C=	GRCh38
NC_000001.10:g.171168584C= , CM000663.1:g.171168584C=	GRCh37
NC_000001.9:g.169435208C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209929.10:c.584C= MANE Select	ENSP00000209929.8:p.Ser195=
ENST00000209929.9:c.584C=	ENSP00000209929.8:p.Ser195=
ENST00000489354.3:n.349C=
ENST00000529935.5:c.412+2634C=	ENSP00000487002.1:n.412+2634C=
NM_001301347.1:c.-34+2634C=	NP_001288276.1:n.-34+2634C=
NM_001460.4:c.584C=	NP_001451.2:p.Ser195=
XR_426768.2:n.701C=
XR_921761.1:n.701C=
XR_922278.1:n.508-31257G=
NM_001365900.1:c.389C=	NP_001352829.1:p.Ser130=
NR_158622.1:n.604C=
XR_001737072.2:n.651C=
XR_001738291.2:n.1307-31257G=
XR_921761.3:n.651C=
XR_922278.3:n.1307-31257G=
NM_001460.5:c.584C= MANE Select	NP_001451.2:p.Ser195=
NR_160266.1:n.512C=
NM_001301347.2:c.-34+2634C=	NP_001288276.1:n.-34+2634C=