Canonical Allele Identifier: CA345429972

Gene: FMN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240092738A>G , CM000663.2:g.240092738A>G	GRCh38
NC_000001.10:g.240256038A>G , CM000663.1:g.240256038A>G	GRCh37
NC_000001.9:g.238322661A>G	NCBI36
NG_042054.1:g.5854A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020066.5:c.629A>G MANE Select	NP_064450.3:p.Gln210Arg
ENST00000319653.14:c.629A>G MANE Select	ENSP00000318884.9:p.Gln210Arg
NM_001305424.1:c.629A>G	NP_001292353.1:p.Gln210Arg
NM_001305424.2:c.629A>G	NP_001292353.1:p.Gln210Arg
NM_001348094.1:c.629A>G	NP_001335023.1:p.Gln210Arg
NM_001348094.2:c.629A>G	NP_001335023.1:p.Gln210Arg
NM_020066.4:c.629A>G	NP_064450.3:p.Gln210Arg
ENST00000319653.13:c.629A>G	ENSP00000318884.9:p.Gln210Arg
ENST00000447095.5:c.-87+24665A>G	ENSP00000409308.1:n.-87+24665A>G
XM_011544237.1:c.629A>G	XP_011542539.1:p.Gln210Arg
XM_011544237.3:c.629A>G	XP_011542539.1:p.Gln210Arg
XM_017001837.1:c.629A>G	XP_016857326.1:p.Gln210Arg
XM_017001838.1:c.629A>G	XP_016857327.1:p.Gln210Arg
XR_949151.1:n.850A>G