Canonical Allele Identifier: CA145916
Gene: MAOA HGNC NCBI

Linked Data

ClinVar Variation Id: 92664
dbSNP Id: rs6323
gnomAD v2: X-43591036-G-T
gnomAD v3: X-43731789-G-T
gnomAD v4: X-43731789-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43731789G>T , CM000685.2:g.43731789G>T GRCh38
NC_000023.10:g.43591036G>T , CM000685.1:g.43591036G>T GRCh37
NC_000023.9:g.43475980G>T NCBI36
NG_008957.2:g.80629G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000542639.6:c.492G>T ENSP00000440846.1:p.Arg164=
ENST00000686683.1:c.201G>T ENSP00000509063.1:p.Arg67=
ENST00000686980.1:n.1023G>T
ENST00000688006.1:c.492G>T ENSP00000510311.1:p.Arg164=
ENST00000688859.1:n.447G>T
ENST00000689087.1:c.492G>T ENSP00000508997.1:p.Arg164=
ENST00000693128.1:c.786G>T ENSP00000508493.1:p.Arg262=
ENST00000338702.4:c.891G>T MANE Select ENSP00000340684.3:p.Arg297=
ENST00000338702.3:c.891G>T ENSP00000340684.3:p.Arg297=
ENST00000542639.5:c.492G>T ENSP00000440846.1:p.Arg164=
NM_000240.3:c.891G>T NP_000231.1:p.Arg297=
NM_001270458.1:c.492G>T NP_001257387.1:p.Arg164=
NM_000240.4:c.891G>T MANE Select NP_000231.1:p.Arg297=
NM_001270458.2:c.492G>T NP_001257387.1:p.Arg164=