Canonical Allele Identifier: CA343187443

Gene: FMO3

Linked Data

• dbSNP Id: rs909530
• MyVariant Identifiers: chr1:g.171083174C>A (hg19) ; chr1:g.171114034C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171114034C>A , CM000663.2:g.171114034C>A	GRCh38
NC_000001.10:g.171083174C>A , CM000663.1:g.171083174C>A	GRCh37
NC_000001.9:g.169349798C>A	NCBI36
NG_012690.1:g.28157C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367755.9:c.855C>A MANE Select	ENSP00000356729.4:p.Asn285Lys
ENST00000367755.8:c.855C>A	ENSP00000356729.4:p.Asn285Lys
NM_001002294.2:c.855C>A	NP_001002294.1:p.Asn285Lys
NM_006894.5:c.855C>A	NP_008825.4:p.Asn285Lys
XM_005245044.1:c.666C>A	XP_005245101.1:p.Asn222Lys
XM_011509345.1:c.795C>A	XP_011507647.1:p.Asn265Lys
XM_011509346.1:c.795C>A	XP_011507648.1:p.Asn265Lys
NM_001319173.1:c.795C>A	NP_001306102.1:p.Asn265Lys
NM_001319174.1:c.666C>A	NP_001306103.1:p.Asn222Lys
XM_011509345.3:c.795C>A	XP_011507647.1:p.Asn265Lys
XM_024454365.1:c.108C>A	XP_024310133.1:p.Asn36Lys
NM_001002294.3:c.855C>A MANE Select	NP_001002294.1:p.Asn285Lys
NM_001319173.2:c.795C>A	NP_001306102.1:p.Asn265Lys
NM_001319174.2:c.666C>A	NP_001306103.1:p.Asn222Lys
NM_006894.6:c.855C>A	NP_008825.4:p.Asn285Lys