Canonical Allele Identifier: CA10391032

Gene: MAOB

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43767565G>A , CM000685.2:g.43767565G>A	GRCh38
NC_000023.10:g.43626812G>A , CM000685.1:g.43626812G>A	GRCh37
NC_000023.9:g.43511756G>A	NCBI36
NG_008723.1:g.119910C>T
NG_008723.2:g.119911C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378069.5:c.1464C>T MANE Select	ENSP00000367309.4:p.Ser488=
ENST00000378069.4:c.1464C>T	ENSP00000367309.4:p.Ser488=
NM_000898.4:c.1464C>T	NP_000889.3:p.Ser488=
XM_005272607.3:c.1416C>T	XP_005272664.1:p.Ser472=
XM_005272608.2:c.1416C>T	XP_005272665.1:p.Ser472=
XM_011543914.1:c.1326C>T	XP_011542216.1:p.Ser442=
XM_005272608.3:c.1416C>T	XP_005272665.1:p.Ser472=
XM_017029523.1:c.1416C>T	XP_016885012.1:p.Ser472=
XM_017029524.2:c.1416C>T	XP_016885013.1:p.Ser472=
NM_000898.5:c.1464C>T MANE Select	NP_000889.3:p.Ser488=