Canonical Allele Identifier: CA345432448

Gene: FMN2

Linked Data

• dbSNP Id: rs1341396589
• gnomAD v3: 1-240123329-A-C
• gnomAD v4: 1-240123329-A-C
• MyVariant Identifiers: chr1:g.240286629A>C (hg19) ; chr1:g.240123329A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240123329A>C , CM000663.2:g.240123329A>C	GRCh38
NC_000001.10:g.240286629A>C , CM000663.1:g.240286629A>C	GRCh37
NC_000001.9:g.238353252A>C	NCBI36
NG_042054.1:g.36445A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000319653.14:c.1766A>C MANE Select	ENSP00000318884.9:p.Asn589Thr
ENST00000681210.1:c.65A>C	ENSP00000505131.1:p.Asn22Thr
ENST00000681741.1:c.65A>C	ENSP00000505116.1:p.Asn22Thr
ENST00000681824.1:c.65A>C	ENSP00000505818.1:p.Asn22Thr
ENST00000319653.13:c.1766A>C	ENSP00000318884.9:p.Asn589Thr
ENST00000447095.5:c.65A>C	ENSP00000409308.1:p.Asn22Thr
NM_001305424.1:c.1766A>C	NP_001292353.1:p.Asn589Thr
NM_020066.4:c.1766A>C	NP_064450.3:p.Asn589Thr
XM_011544237.1:c.1766A>C	XP_011542539.1:p.Asn589Thr
XR_949151.1:n.1987A>C
NM_001348094.1:c.1766A>C	NP_001335023.1:p.Asn589Thr
XM_011544237.3:c.1766A>C	XP_011542539.1:p.Asn589Thr
XM_017001837.1:c.1766A>C	XP_016857326.1:p.Asn589Thr
XM_017001838.1:c.1766A>C	XP_016857327.1:p.Asn589Thr
NM_020066.5:c.1766A>C MANE Select	NP_064450.3:p.Asn589Thr
NM_001305424.2:c.1766A>C	NP_001292353.1:p.Asn589Thr
NM_001348094.2:c.1766A>C	NP_001335023.1:p.Asn589Thr