Canonical Allele Identifier: CA1206795964

Gene: FMO3

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171111474G>T , CM000663.2:g.171111474G>T	GRCh38
NC_000001.10:g.171080615G>T , CM000663.1:g.171080615G>T	GRCh37
NC_000001.9:g.169347239G>T	NCBI36
NG_012690.1:g.25598G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.827+477G>T MANE Select	ENSP00000356729.4:n.827+477G>T
ENST00000367755.8:c.827+477G>T	ENSP00000356729.4:n.827+477G>T
NM_001002294.2:c.827+477G>T	NP_001002294.1:n.827+477G>T
NM_006894.5:c.827+477G>T	NP_008825.4:n.827+477G>T
XM_005245044.1:c.638+477G>T	XP_005245101.1:n.638+477G>T
XM_011509345.1:c.767+477G>T	XP_011507647.1:n.767+477G>T
XM_011509346.1:c.767+477G>T	XP_011507648.1:n.767+477G>T
NM_001319173.1:c.767+477G>T	NP_001306102.1:n.767+477G>T
NM_001319174.1:c.638+477G>T	NP_001306103.1:n.638+477G>T
XM_011509345.3:c.767+477G>T	XP_011507647.1:n.767+477G>T
XM_024454365.1:c.81-2533G>T	XP_024310133.1:n.81-2533G>T
NM_001002294.3:c.827+477G>T MANE Select	NP_001002294.1:n.827+477G>T
NM_001319173.2:c.767+477G>T	NP_001306102.1:n.767+477G>T
NM_001319174.2:c.638+477G>T	NP_001306103.1:n.638+477G>T
NM_006894.6:c.827+477G>T	NP_008825.4:n.827+477G>T