Canonical Allele Identifier: CA343169771

Gene: FMO3

Linked Data

• MyVariant Identifiers: chr1:g.171086285G>C (hg19) ; chr1:g.171117145G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171117145G>C , CM000663.2:g.171117145G>C	GRCh38
NC_000001.10:g.171086285G>C , CM000663.1:g.171086285G>C	GRCh37
NC_000001.9:g.169352909G>C	NCBI36
NG_012690.1:g.31268G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.1302G>C MANE Select	ENSP00000356729.4:p.Met434Ile
ENST00000367755.8:c.1302G>C	ENSP00000356729.4:p.Met434Ile
NM_001002294.2:c.1302G>C	NP_001002294.1:p.Met434Ile
NM_006894.5:c.1302G>C	NP_008825.4:p.Met434Ile
XM_005245044.1:c.1113G>C	XP_005245101.1:p.Met371Ile
XM_011509345.1:c.1242G>C	XP_011507647.1:p.Met414Ile
XM_011509346.1:c.1242G>C	XP_011507648.1:p.Met414Ile
NM_001319173.1:c.1242G>C	NP_001306102.1:p.Met414Ile
NM_001319174.1:c.1113G>C	NP_001306103.1:p.Met371Ile
XM_011509345.3:c.1242G>C	XP_011507647.1:p.Met414Ile
XM_024454365.1:c.555G>C	XP_024310133.1:p.Met185Ile
NM_001002294.3:c.1302G>C MANE Select	NP_001002294.1:p.Met434Ile
NM_001319173.2:c.1242G>C	NP_001306102.1:p.Met414Ile
NM_001319174.2:c.1113G>C	NP_001306103.1:p.Met371Ile
NM_006894.6:c.1302G>C	NP_008825.4:p.Met434Ile