Canonical Allele Identifier: CA343187340

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171114005A>G , CM000663.2:g.171114005A>G	GRCh38
NC_000001.10:g.171083145A>G , CM000663.1:g.171083145A>G	GRCh37
NC_000001.9:g.169349769A>G	NCBI36
NG_012690.1:g.28128A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.828-2A>G MANE Select	NP_001002294.1:n.828-2A>G
ENST00000367755.9:c.828-2A>G MANE Select	ENSP00000356729.4:n.828-2A>G
NM_001002294.2:c.828-2A>G	NP_001002294.1:n.828-2A>G
NM_001319173.1:c.768-2A>G	NP_001306102.1:n.768-2A>G
NM_001319173.2:c.768-2A>G	NP_001306102.1:n.768-2A>G
NM_001319174.1:c.639-2A>G	NP_001306103.1:n.639-2A>G
NM_001319174.2:c.639-2A>G	NP_001306103.1:n.639-2A>G
NM_006894.5:c.828-2A>G	NP_008825.4:n.828-2A>G
NM_006894.6:c.828-2A>G	NP_008825.4:n.828-2A>G
ENST00000367755.8:c.828-2A>G	ENSP00000356729.4:n.828-2A>G
XM_005245044.1:c.639-2A>G	XP_005245101.1:n.639-2A>G
XM_011509345.1:c.768-2A>G	XP_011507647.1:n.768-2A>G
XM_011509345.3:c.768-2A>G	XP_011507647.1:n.768-2A>G
XM_011509346.1:c.768-2A>G	XP_011507648.1:n.768-2A>G
XM_024454365.1:c.81-2A>G	XP_024310133.1:n.81-2A>G