Canonical Allele Identifier: CA343184563

Gene: FMO3

Linked Data

• ClinVar Variation Id: 2263197
• ClinVar RCV Id: RCV002792994
• gnomAD v4: 1-171108104-C-G
• MyVariant Identifiers: chr1:g.171077245C>G (hg19) ; chr1:g.171108104C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171108104C>G , CM000663.2:g.171108104C>G	GRCh38
NC_000001.10:g.171077245C>G , CM000663.1:g.171077245C>G	GRCh37
NC_000001.9:g.169343869C>G	NCBI36
NG_012690.1:g.22228C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.510C>G MANE Select	ENSP00000356729.4:p.Cys170Trp
ENST00000367755.8:c.510C>G	ENSP00000356729.4:p.Cys170Trp
ENST00000479749.1:c.468-12C>G	ENSP00000477451.1:n.468-12C>G
NM_001002294.2:c.510C>G	NP_001002294.1:p.Cys170Trp
NM_006894.5:c.510C>G	NP_008825.4:p.Cys170Trp
XM_005245044.1:c.321C>G	XP_005245101.1:p.Cys107Trp
XM_011509345.1:c.450C>G	XP_011507647.1:p.Cys150Trp
XM_011509346.1:c.450C>G	XP_011507648.1:p.Cys150Trp
NM_001319173.1:c.450C>G	NP_001306102.1:p.Cys150Trp
NM_001319174.1:c.321C>G	NP_001306103.1:p.Cys107Trp
XM_011509345.3:c.450C>G	XP_011507647.1:p.Cys150Trp
XM_024454365.1:c.-38C>G	XP_024310133.1:n.-38C>G
NM_001002294.3:c.510C>G MANE Select	NP_001002294.1:p.Cys170Trp
NM_001319173.2:c.450C>G	NP_001306102.1:p.Cys150Trp
NM_001319174.2:c.321C>G	NP_001306103.1:p.Cys107Trp
NM_006894.6:c.510C>G	NP_008825.4:p.Cys170Trp