Canonical Allele Identifier: CA16603456
Gene: FMO3 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171114038G>T , CM000663.2:g.171114038G>T GRCh38
NC_000001.10:g.171083178G>T , CM000663.1:g.171083178G>T GRCh37
NC_000001.9:g.169349802G>T NCBI36
NG_012690.1:g.28161G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367755.9:c.859G>T MANE Select ENSP00000356729.4:p.Glu287Ter
ENST00000367755.8:c.859G>T ENSP00000356729.4:p.Glu287Ter
NM_001002294.2:c.859G>T NP_001002294.1:p.Glu287Ter
NM_006894.5:c.859G>T NP_008825.4:p.Glu287Ter
XM_005245044.1:c.670G>T XP_005245101.1:p.Glu224Ter
XM_011509345.1:c.799G>T XP_011507647.1:p.Glu267Ter
XM_011509346.1:c.799G>T XP_011507648.1:p.Glu267Ter
NM_001319173.1:c.799G>T NP_001306102.1:p.Glu267Ter
NM_001319174.1:c.670G>T NP_001306103.1:p.Glu224Ter
XM_011509345.3:c.799G>T XP_011507647.1:p.Glu267Ter
XM_024454365.1:c.112G>T XP_024310133.1:p.Glu38Ter
NM_001002294.3:c.859G>T MANE Select NP_001002294.1:p.Glu287Ter
NM_001319173.2:c.799G>T NP_001306102.1:p.Glu267Ter
NM_001319174.2:c.670G>T NP_001306103.1:p.Glu224Ter
NM_006894.6:c.859G>T NP_008825.4:p.Glu287Ter