Canonical Allele Identifier: CA1240770

Gene: FMO3

Linked Data

• ClinVar Variation Id: 293695
• ClinVar RCV Id: RCV000307703 ; RCV000911384
• dbSNP Id: rs141117096
• ExAC: 1:171085368 A / G
• gnomAD v2: 1-171085368-A-G
• gnomAD v3: 1-171116228-A-G
• gnomAD v4: 1-171116228-A-G
• MyVariant Identifiers: chr1:g.171085368A>G (hg19) ; chr1:g.171116228A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171116228A>G , CM000663.2:g.171116228A>G	GRCh38
NC_000001.10:g.171085368A>G , CM000663.1:g.171085368A>G	GRCh37
NC_000001.9:g.169351992A>G	NCBI36
NG_012690.1:g.30351A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.1204A>G MANE Select	ENSP00000356729.4:p.Met402Val
ENST00000367755.8:c.1204A>G	ENSP00000356729.4:p.Met402Val
NM_001002294.2:c.1204A>G	NP_001002294.1:p.Met402Val
NM_006894.5:c.1204A>G	NP_008825.4:p.Met402Val
XM_005245044.1:c.1015A>G	XP_005245101.1:p.Met339Val
XM_011509345.1:c.1144A>G	XP_011507647.1:p.Met382Val
XM_011509346.1:c.1144A>G	XP_011507648.1:p.Met382Val
NM_001319173.1:c.1144A>G	NP_001306102.1:p.Met382Val
NM_001319174.1:c.1015A>G	NP_001306103.1:p.Met339Val
XM_011509345.3:c.1144A>G	XP_011507647.1:p.Met382Val
XM_024454365.1:c.457A>G	XP_024310133.1:p.Met153Val
NM_001002294.3:c.1204A>G MANE Select	NP_001002294.1:p.Met402Val
NM_001319173.2:c.1144A>G	NP_001306102.1:p.Met382Val
NM_001319174.2:c.1015A>G	NP_001306103.1:p.Met339Val
NM_006894.6:c.1204A>G	NP_008825.4:p.Met402Val