Canonical Allele Identifier: CA343188034

Gene: FMO3

Linked Data

• MyVariant Identifiers: chr1:g.171083401T>G (hg19) ; chr1:g.171114261T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171114261T>G , CM000663.2:g.171114261T>G	GRCh38
NC_000001.10:g.171083401T>G , CM000663.1:g.171083401T>G	GRCh37
NC_000001.9:g.169350025T>G	NCBI36
NG_012690.1:g.28384T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367755.9:c.1082T>G MANE Select	ENSP00000356729.4:p.Leu361Arg
ENST00000367755.8:c.1082T>G	ENSP00000356729.4:p.Leu361Arg
NM_001002294.2:c.1082T>G	NP_001002294.1:p.Leu361Arg
NM_006894.5:c.1082T>G	NP_008825.4:p.Leu361Arg
XM_005245044.1:c.893T>G	XP_005245101.1:p.Leu298Arg
XM_011509345.1:c.1022T>G	XP_011507647.1:p.Leu341Arg
XM_011509346.1:c.1022T>G	XP_011507648.1:p.Leu341Arg
NM_001319173.1:c.1022T>G	NP_001306102.1:p.Leu341Arg
NM_001319174.1:c.893T>G	NP_001306103.1:p.Leu298Arg
XM_011509345.3:c.1022T>G	XP_011507647.1:p.Leu341Arg
XM_024454365.1:c.335T>G	XP_024310133.1:p.Leu112Arg
NM_001002294.3:c.1082T>G MANE Select	NP_001002294.1:p.Leu361Arg
NM_001319173.2:c.1022T>G	NP_001306102.1:p.Leu341Arg
NM_001319174.2:c.893T>G	NP_001306103.1:p.Leu298Arg
NM_006894.6:c.1082T>G	NP_008825.4:p.Leu361Arg