Canonical Allele Identifier: CA32540349

Gene: FMO2

Linked Data

• dbSNP Id: rs2020865
• gnomAD v3: 1-171207773-T-C
• gnomAD v4: 1-171207773-T-C
• MyVariant Identifiers: chr1:g.171176912T>C (hg19) ; chr1:g.171207773T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171207773T>C , CM000663.2:g.171207773T>C	GRCh38
NC_000001.10:g.171176912T>C , CM000663.1:g.171176912T>C	GRCh37
NC_000001.9:g.169443536T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000209929.10:c.1239T>C MANE Select	ENSP00000209929.8:p.Asn413=
ENST00000209929.9:c.1239T>C	ENSP00000209929.8:p.Asn413=
ENST00000488431.1:n.231T>C
ENST00000529935.5:c.1024T>C	ENSP00000487002.1:n.1024T>C
NM_001301347.1:c.579T>C	NP_001288276.1:p.Asn193=
NM_001460.4:c.1239T>C	NP_001451.2:p.Asn413=
XR_426768.2:n.1356T>C
XR_921761.1:n.1356T>C
XR_922278.1:n.508-39585A>G
NM_001365900.1:c.1044T>C	NP_001352829.1:p.Asn348=
NR_158622.1:n.1259T>C
XR_001737072.2:n.1306T>C
XR_001738291.2:n.1307-39585A>G
XR_921761.3:n.1306T>C
XR_922278.3:n.1307-39585A>G
NM_001460.5:c.1239T>C MANE Select	NP_001451.2:p.Asn413=
NR_160266.1:n.1167T>C
NM_001301347.2:c.579T>C	NP_001288276.1:p.Asn193=