Canonical Allele Identifier: CA2426703367

Gene: MAOB

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43829718A>T , CM000685.2:g.43829718A>T	GRCh38
NC_000023.10:g.43688964A>T , CM000685.1:g.43688964A>T	GRCh37
NC_000023.9:g.43573908A>T	NCBI36
NG_008723.1:g.57758T>A
NG_008723.2:g.57758T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378069.5:c.279+9150T>A MANE Select	ENSP00000367309.4:n.279+9150T>A
ENST00000378069.4:c.279+9150T>A	ENSP00000367309.4:n.279+9150T>A
ENST00000487544.1:n.605+9150T>A
NM_000898.4:c.279+9150T>A	NP_000889.3:n.279+9150T>A
XM_005272607.3:c.231+9150T>A	XP_005272664.1:n.231+9150T>A
XM_005272608.2:c.231+9150T>A	XP_005272665.1:n.231+9150T>A
XM_011543914.1:c.141+13952T>A	XP_011542216.1:n.141+13952T>A
XM_005272608.3:c.231+9150T>A	XP_005272665.1:n.231+9150T>A
XM_017029523.1:c.231+9150T>A	XP_016885012.1:n.231+9150T>A
XM_017029524.2:c.231+9150T>A	XP_016885013.1:n.231+9150T>A
NM_000898.5:c.279+9150T>A MANE Select	NP_000889.3:n.279+9150T>A