Canonical Allele Identifier: CA2426682229

Gene: MAOB

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43768752T= , CM000685.2:g.43768752T=	GRCh38
NC_000023.10:g.43627999T= , CM000685.1:g.43627999T=	GRCh37
NC_000023.9:g.43512943T=	NCBI36
NG_008723.1:g.118723A=
NG_008723.2:g.118724A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000898.5:c.1348-36A= MANE Select	NP_000889.3:n.1348-36A=
ENST00000378069.5:c.1348-36A= MANE Select	ENSP00000367309.4:n.1348-36A=
NM_000898.4:c.1348-36A=	NP_000889.3:n.1348-36A=
ENST00000378069.4:c.1348-36A=	ENSP00000367309.4:n.1348-36A=
XM_005272607.3:c.1300-36A=	XP_005272664.1:n.1300-36A=
XM_005272608.2:c.1300-36A=	XP_005272665.1:n.1300-36A=
XM_005272608.3:c.1300-36A=	XP_005272665.1:n.1300-36A=
XM_011543914.1:c.1210-36A=	XP_011542216.1:n.1210-36A=
XM_017029523.1:c.1300-36A=	XP_016885012.1:n.1300-36A=
XM_017029524.2:c.1300-36A=	XP_016885013.1:n.1300-36A=