Canonical Allele Identifier: CA2426684241

Gene: MAOB

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43774493G= , CM000685.2:g.43774493G=	GRCh38
NC_000023.10:g.43633740G= , CM000685.1:g.43633740G=	GRCh37
NC_000023.9:g.43518684G=	NCBI36
NG_008723.1:g.112982C=
NG_008723.2:g.112983C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378069.5:c.1235+682C= MANE Select	ENSP00000367309.4:n.1235+682C=
ENST00000378069.4:c.1235+682C=	ENSP00000367309.4:n.1235+682C=
NM_000898.4:c.1235+682C=	NP_000889.3:n.1235+682C=
XM_005272607.3:c.1187+682C=	XP_005272664.1:n.1187+682C=
XM_005272608.2:c.1187+682C=	XP_005272665.1:n.1187+682C=
XM_011543914.1:c.1097+682C=	XP_011542216.1:n.1097+682C=
XM_005272608.3:c.1187+682C=	XP_005272665.1:n.1187+682C=
XM_017029523.1:c.1187+682C=	XP_016885012.1:n.1187+682C=
XM_017029524.2:c.1187+682C=	XP_016885013.1:n.1187+682C=
NM_000898.5:c.1235+682C= MANE Select	NP_000889.3:n.1235+682C=