Canonical Allele Identifier: CA10390882
Gene: MAOA HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2235186

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43736181A>G , CM000685.2:g.43736181A>G GRCh38
NC_000023.10:g.43595428A>G , CM000685.1:g.43595428A>G GRCh37
NC_000023.9:g.43480372A>G NCBI36
NG_008957.2:g.85021A>G

Transcript Alleles

HGVS Amino-acid change
NM_000240.3:c.1053-46A>G VV NP_000231.1:p.=
NM_001270458.1:c.654-46A>G VV NP_001257387.1:p.=
ENST00000338702.3:c.1053-46A>G ENSP00000340684.3:p.=
ENST00000542639.5:c.654-46A>G ENSP00000440846.1:p.=