Canonical Allele Identifier: CA15006399
Gene: MAOA HGNC NCBI

Linked Data

dbSNP Id: rs3027400
gnomAD v2: X-43592763-T-G
gnomAD v3: X-43733516-T-G
gnomAD v4: X-43733516-T-G
MyVariant Identifiers: chrX:g.43592763T>G (hg19) chrX:g.43733516T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43733516T>G , CM000685.2:g.43733516T>G GRCh38
NC_000023.10:g.43592763T>G , CM000685.1:g.43592763T>G GRCh37
NC_000023.9:g.43477707T>G NCBI36
NG_008957.2:g.82356T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000542639.6:c.653+721T>G ENSP00000440846.1:n.653+721T>G
ENST00000686683.1:c.362+721T>G ENSP00000509063.1:n.362+721T>G
ENST00000686980.1:n.1184+721T>G
ENST00000688006.1:c.653+721T>G ENSP00000510311.1:n.653+721T>G
ENST00000688859.1:n.608+721T>G
ENST00000689087.1:c.653+721T>G ENSP00000508997.1:n.653+721T>G
ENST00000693128.1:c.947+721T>G ENSP00000508493.1:n.947+721T>G
ENST00000338702.4:c.1052+721T>G MANE Select ENSP00000340684.3:n.1052+721T>G
ENST00000338702.3:c.1052+721T>G ENSP00000340684.3:n.1052+721T>G
ENST00000542639.5:c.653+721T>G ENSP00000440846.1:n.653+721T>G
NM_000240.3:c.1052+721T>G NP_000231.1:n.1052+721T>G
NM_001270458.1:c.653+721T>G NP_001257387.1:n.653+721T>G
NM_000240.4:c.1052+721T>G MANE Select NP_000231.1:n.1052+721T>G
NM_001270458.2:c.653+721T>G NP_001257387.1:n.653+721T>G
Search 100 bp 5'
Search 100 bp 3'