Canonical Allele Identifier: CA343188056

Gene: FMO3

Linked Data

• MyVariant Identifiers: chr1:g.171083412A>G (hg19) ; chr1:g.171114272A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171114272A>G , CM000663.2:g.171114272A>G	GRCh38
NC_000001.10:g.171083412A>G , CM000663.1:g.171083412A>G	GRCh37
NC_000001.9:g.169350036A>G	NCBI36
NG_012690.1:g.28395A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.1093A>G MANE Select	ENSP00000356729.4:p.Thr365Ala
ENST00000367755.8:c.1093A>G	ENSP00000356729.4:p.Thr365Ala
NM_001002294.2:c.1093A>G	NP_001002294.1:p.Thr365Ala
NM_006894.5:c.1093A>G	NP_008825.4:p.Thr365Ala
XM_005245044.1:c.904A>G	XP_005245101.1:p.Thr302Ala
XM_011509345.1:c.1033A>G	XP_011507647.1:p.Thr345Ala
XM_011509346.1:c.1033A>G	XP_011507648.1:p.Thr345Ala
NM_001319173.1:c.1033A>G	NP_001306102.1:p.Thr345Ala
NM_001319174.1:c.904A>G	NP_001306103.1:p.Thr302Ala
XM_011509345.3:c.1033A>G	XP_011507647.1:p.Thr345Ala
XM_024454365.1:c.346A>G	XP_024310133.1:p.Thr116Ala
NM_001002294.3:c.1093A>G MANE Select	NP_001002294.1:p.Thr365Ala
NM_001319173.2:c.1033A>G	NP_001306102.1:p.Thr345Ala
NM_001319174.2:c.904A>G	NP_001306103.1:p.Thr302Ala
NM_006894.6:c.1093A>G	NP_008825.4:p.Thr365Ala