Canonical Allele Identifier: CA641640543

Gene: MAOA

Linked Data

• dbSNP Id: rs1298783282
• gnomAD v2: X-43553211-T-C
• gnomAD v3: X-43693964-T-C
• gnomAD v4: X-43693964-T-C
• MyVariant Identifiers: chrX:g.43553211T>C (hg19) ; chrX:g.43693964T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.43693964T>C , CM000685.2:g.43693964T>C	GRCh38
NC_000023.10:g.43553211T>C , CM000685.1:g.43553211T>C	GRCh37
NC_000023.9:g.43438155T>C	NCBI36
NG_008957.2:g.42804T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000497485.2:n.974T>C
ENST00000542639.6:c.-94+536T>C	ENSP00000440846.1:n.-94+536T>C
ENST00000686683.1:c.-305+536T>C	ENSP00000509063.1:n.-305+536T>C
ENST00000686980.1:n.438+536T>C
ENST00000688006.1:c.-94+536T>C	ENSP00000510311.1:n.-94+536T>C
ENST00000689087.1:c.-94+536T>C	ENSP00000508997.1:n.-94+536T>C
ENST00000693128.1:c.306+536T>C	ENSP00000508493.1:n.306+536T>C
ENST00000338702.4:c.306+536T>C MANE Select	ENSP00000340684.3:n.306+536T>C
ENST00000338702.3:c.306+536T>C	ENSP00000340684.3:n.306+536T>C
ENST00000497485.1:n.454+536T>C
ENST00000542639.5:c.-94+536T>C	ENSP00000440846.1:n.-94+536T>C
NM_000240.3:c.306+536T>C	NP_000231.1:n.306+536T>C
NM_001270458.1:c.-94+536T>C	NP_001257387.1:n.-94+536T>C
NM_000240.4:c.306+536T>C MANE Select	NP_000231.1:n.306+536T>C
NM_001270458.2:c.-94+536T>C	NP_001257387.1:n.-94+536T>C