Canonical Allele Identifier: CA32542605

Gene: FMO3

Linked Data

• dbSNP Id: rs72549323
• MyVariant Identifiers: chr1:g.171072991G>C (hg19) ; chr1:g.171103850G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171103850G>C , CM000663.2:g.171103850G>C	GRCh38
NC_000001.10:g.171072991G>C , CM000663.1:g.171072991G>C	GRCh37
NC_000001.9:g.169339615G>C	NCBI36
NG_012690.1:g.17974G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.198G>C MANE Select	ENSP00000356729.4:p.Met66Ile
ENST00000367755.8:c.198G>C	ENSP00000356729.4:p.Met66Ile
ENST00000472784.5:c.*178G>C	ENSP00000476963.1:n.*178G>C
ENST00000478457.1:n.511G>C
ENST00000479749.1:c.198G>C	ENSP00000477451.1:p.Met66Ile
NM_001002294.2:c.198G>C	NP_001002294.1:p.Met66Ile
NM_006894.5:c.198G>C	NP_008825.4:p.Met66Ile
XM_005245044.1:c.133-3825G>C	XP_005245101.1:n.133-3825G>C
XM_011509345.1:c.138G>C	XP_011507647.1:p.Met46Ile
XM_011509346.1:c.138G>C	XP_011507648.1:p.Met46Ile
NM_001319173.1:c.138G>C	NP_001306102.1:p.Met46Ile
NM_001319174.1:c.133-3825G>C	NP_001306103.1:n.133-3825G>C
XM_011509345.3:c.138G>C	XP_011507647.1:p.Met46Ile
NM_001002294.3:c.198G>C MANE Select	NP_001002294.1:p.Met66Ile
NM_001319173.2:c.138G>C	NP_001306102.1:p.Met46Ile
NM_001319174.2:c.133-3825G>C	NP_001306103.1:n.133-3825G>C
NM_006894.6:c.198G>C	NP_008825.4:p.Met66Ile