Canonical Allele Identifier: CA343183869

Gene: FMO3

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171107795G>C , CM000663.2:g.171107795G>C	GRCh38
NC_000001.10:g.171076936G>C , CM000663.1:g.171076936G>C	GRCh37
NC_000001.9:g.169343560G>C	NCBI36
NG_012690.1:g.21919G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.442G>C MANE Select	ENSP00000356729.4:p.Gly148Arg
ENST00000367755.8:c.442G>C	ENSP00000356729.4:p.Gly148Arg
ENST00000479749.1:c.442G>C	ENSP00000477451.1:p.Gly148Arg
NM_001002294.2:c.442G>C	NP_001002294.1:p.Gly148Arg
NM_006894.5:c.442G>C	NP_008825.4:p.Gly148Arg
XM_005245044.1:c.253G>C	XP_005245101.1:p.Gly85Arg
XM_011509345.1:c.382G>C	XP_011507647.1:p.Gly128Arg
XM_011509346.1:c.382G>C	XP_011507648.1:p.Gly128Arg
NM_001319173.1:c.382G>C	NP_001306102.1:p.Gly128Arg
NM_001319174.1:c.253G>C	NP_001306103.1:p.Gly85Arg
XM_011509345.3:c.382G>C	XP_011507647.1:p.Gly128Arg
XM_024454365.1:c.-106G>C	XP_024310133.1:n.-106G>C
NM_001002294.3:c.442G>C MANE Select	NP_001002294.1:p.Gly148Arg
NM_001319173.2:c.382G>C	NP_001306102.1:p.Gly128Arg
NM_001319174.2:c.253G>C	NP_001306103.1:p.Gly85Arg
NM_006894.6:c.442G>C	NP_008825.4:p.Gly148Arg