Canonical Allele Identifier: CA343175810

Gene: FMO2

Linked Data

• dbSNP Id: rs2020862
• MyVariant Identifiers: chr1:g.171168584C>A (hg19) ; chr1:g.171199445C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171199445C>A , CM000663.2:g.171199445C>A	GRCh38
NC_000001.10:g.171168584C>A , CM000663.1:g.171168584C>A	GRCh37
NC_000001.9:g.169435208C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000209929.10:c.584C>A MANE Select	ENSP00000209929.8:p.Ser195Ter
ENST00000209929.9:c.584C>A	ENSP00000209929.8:p.Ser195Ter
ENST00000489354.3:n.349C>A
ENST00000529935.5:c.412+2634C>A	ENSP00000487002.1:n.412+2634C>A
NM_001301347.1:c.-34+2634C>A	NP_001288276.1:n.-34+2634C>A
NM_001460.4:c.584C>A	NP_001451.2:p.Ser195Ter
XR_426768.2:n.701C>A
XR_921761.1:n.701C>A
XR_922278.1:n.508-31257G>T
NM_001365900.1:c.389C>A	NP_001352829.1:p.Ser130Ter
NR_158622.1:n.604C>A
XR_001737072.2:n.651C>A
XR_001738291.2:n.1307-31257G>T
XR_921761.3:n.651C>A
XR_922278.3:n.1307-31257G>T
NM_001460.5:c.584C>A MANE Select	NP_001451.2:p.Ser195Ter
NR_160266.1:n.512C>A
NM_001301347.2:c.-34+2634C>A	NP_001288276.1:n.-34+2634C>A