Canonical Allele Identifier: CA1140178194
Gene: FMN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240392735T= , CM000663.2:g.240392735T= GRCh38
NC_000001.10:g.240556035T= , CM000663.1:g.240556035T= GRCh37
NC_000001.9:g.238622658T= NCBI36
NG_042054.1:g.305851T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000319653.14:c.4910+173T= MANE Select ENSP00000318884.9:n.4910+173T=
ENST00000545751.3:c.751+173T=
ENST00000679390.1:n.1172+173T=
ENST00000679646.1:n.4376+173T=
ENST00000679980.1:c.1179+173T=
ENST00000681131.1:c.910+173T=
ENST00000681210.1:c.1130+173T= ENSP00000505131.1:n.1130+173T=
ENST00000681296.1:n.2097+173T=
ENST00000681741.1:c.*954+173T= ENSP00000505116.1:n.*954+173T=
ENST00000681805.1:c.795+173T=
ENST00000681824.1:c.1037+173T= ENSP00000505818.1:n.1037+173T=
ENST00000319653.13:c.4910+173T= ENSP00000318884.9:n.4910+173T=
ENST00000545751.2:c.338+173T= ENSP00000437918.2:n.338+173T=
NM_001305424.1:c.4922+173T= NP_001292353.1:n.4922+173T=
NM_020066.4:c.4910+173T= NP_064450.3:n.4910+173T=
NM_001348094.1:c.2738+173T= NP_001335023.1:n.2738+173T=
XM_017001840.2:c.3050+173T= XP_016857329.1:n.3050+173T=
XM_017001841.2:c.3050+173T= XP_016857330.1:n.3050+173T=
NM_020066.5:c.4910+173T= MANE Select NP_064450.3:n.4910+173T=
NM_001305424.2:c.4922+173T= NP_001292353.1:n.4922+173T=
NM_001348094.2:c.2738+173T= NP_001335023.1:n.2738+173T=