Canonical Allele Identifier: CA1229143855

Gene: FMN2

Linked Data

• dbSNP Id: rs1676470430

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240462180C>A , CM000663.2:g.240462180C>A	GRCh38
NC_000001.10:g.240625480C>A , CM000663.1:g.240625480C>A	GRCh37
NC_000001.9:g.238692103C>A	NCBI36
NG_042054.1:g.375296C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000319653.14:c.5061-10192C>A MANE Select	ENSP00000318884.9:n.5061-10192C>A
ENST00000543681.2:n.1951+2737C>A
ENST00000545751.3:c.902-10192C>A
ENST00000679390.1:n.1323-10192C>A
ENST00000679646.1:n.4527-10192C>A
ENST00000679980.1:c.1330-10192C>A
ENST00000681131.1:c.1061-10192C>A
ENST00000681210.1:c.1281-10192C>A	ENSP00000505131.1:n.1281-10192C>A
ENST00000681296.1:n.2248-10192C>A
ENST00000681741.1:c.*1105-10192C>A	ENSP00000505116.1:n.*1105-10192C>A
ENST00000681805.1:c.1128-10192C>A
ENST00000681824.1:c.1188-10192C>A	ENSP00000505818.1:n.1188-10192C>A
ENST00000319653.13:c.5061-10192C>A	ENSP00000318884.9:n.5061-10192C>A
ENST00000543681.1:c.-699+2737C>A	ENSP00000439136.1:n.-699+2737C>A
ENST00000545751.2:c.489-10192C>A	ENSP00000437918.2:n.489-10192C>A
NM_001305424.1:c.5073-10192C>A	NP_001292353.1:n.5073-10192C>A
NM_020066.4:c.5061-10192C>A	NP_064450.3:n.5061-10192C>A
NM_001348094.1:c.2889-10192C>A	NP_001335023.1:n.2889-10192C>A
XM_017001840.2:c.3201-10192C>A	XP_016857329.1:n.3201-10192C>A
XM_017001841.2:c.3201-10192C>A	XP_016857330.1:n.3201-10192C>A
NM_020066.5:c.5061-10192C>A MANE Select	NP_064450.3:n.5061-10192C>A
NM_001305424.2:c.5073-10192C>A	NP_001292353.1:n.5073-10192C>A
NM_001348094.2:c.2889-10192C>A	NP_001335023.1:n.2889-10192C>A