Canonical Allele Identifier: CA343184275

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171107839T>G , CM000663.2:g.171107839T>G	GRCh38
NC_000001.10:g.171076980T>G , CM000663.1:g.171076980T>G	GRCh37
NC_000001.9:g.169343604T>G	NCBI36
NG_012690.1:g.21963T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.484+2T>G MANE Select	NP_001002294.1:n.484+2T>G
ENST00000367755.9:c.484+2T>G MANE Select	ENSP00000356729.4:n.484+2T>G
NM_001002294.2:c.484+2T>G	NP_001002294.1:n.484+2T>G
NM_001319173.1:c.424+2T>G	NP_001306102.1:n.424+2T>G
NM_001319173.2:c.424+2T>G	NP_001306102.1:n.424+2T>G
NM_001319174.1:c.295+2T>G	NP_001306103.1:n.295+2T>G
NM_001319174.2:c.295+2T>G	NP_001306103.1:n.295+2T>G
NM_006894.5:c.484+2T>G	NP_008825.4:n.484+2T>G
NM_006894.6:c.484+2T>G	NP_008825.4:n.484+2T>G
ENST00000367755.8:c.484+2T>G	ENSP00000356729.4:n.484+2T>G
ENST00000479749.1:c.467+19T>G	ENSP00000477451.1:n.467+19T>G
XM_005245044.1:c.295+2T>G	XP_005245101.1:n.295+2T>G
XM_011509345.1:c.424+2T>G	XP_011507647.1:n.424+2T>G
XM_011509345.3:c.424+2T>G	XP_011507647.1:n.424+2T>G
XM_011509346.1:c.424+2T>G	XP_011507648.1:n.424+2T>G
XM_024454365.1:c.-64+2T>G	XP_024310133.1:n.-64+2T>G