Canonical Allele Identifier: CA875544966

Gene: MAOB

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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