Canonical Allele Identifier: CA2426699763

Gene: MAOB

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43818795G= , CM000685.2:g.43818795G=	GRCh38
NC_000023.10:g.43678042G= , CM000685.1:g.43678042G=	GRCh37
NC_000023.9:g.43562986G=	NCBI36
NG_008723.1:g.68680C=
NG_008723.2:g.68681C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378069.5:c.280-15391C= MANE Select	ENSP00000367309.4:n.280-15391C=
ENST00000378069.4:c.280-15391C=	ENSP00000367309.4:n.280-15391C=
ENST00000487544.1:n.606-15391C=
NM_000898.4:c.280-15391C=	NP_000889.3:n.280-15391C=
XM_005272607.3:c.232-15391C=	XP_005272664.1:n.232-15391C=
XM_005272608.2:c.232-15391C=	XP_005272665.1:n.232-15391C=
XM_011543914.1:c.142-15391C=	XP_011542216.1:n.142-15391C=
XM_005272608.3:c.232-15391C=	XP_005272665.1:n.232-15391C=
XM_017029523.1:c.232-15391C=	XP_016885012.1:n.232-15391C=
XM_017029524.2:c.232-15391C=	XP_016885013.1:n.232-15391C=
NM_000898.5:c.280-15391C= MANE Select	NP_000889.3:n.280-15391C=