Canonical Allele Identifier: CA40317294
Gene: FMN2 HGNC NCBI

Linked Data

dbSNP Id: rs888679267

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240396187G>A , CM000663.2:g.240396187G>A GRCh38
NC_000001.10:g.240559487G>A , CM000663.1:g.240559487G>A GRCh37
NC_000001.9:g.238626110G>A NCBI36
NG_042054.1:g.309303G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000319653.14:c.4910+3625G>A MANE Select ENSP00000318884.9:n.4910+3625G>A
ENST00000545751.3:c.751+3625G>A
ENST00000679390.1:n.1172+3625G>A
ENST00000679646.1:n.4376+3625G>A
ENST00000679980.1:c.1179+3625G>A
ENST00000681131.1:c.910+3625G>A
ENST00000681210.1:c.1130+3625G>A ENSP00000505131.1:n.1130+3625G>A
ENST00000681296.1:n.2097+3625G>A
ENST00000681741.1:c.*954+3625G>A ENSP00000505116.1:n.*954+3625G>A
ENST00000681805.1:c.795+3625G>A
ENST00000681824.1:c.1037+3625G>A ENSP00000505818.1:n.1037+3625G>A
ENST00000319653.13:c.4910+3625G>A ENSP00000318884.9:n.4910+3625G>A
ENST00000545751.2:c.338+3625G>A ENSP00000437918.2:n.338+3625G>A
NM_001305424.1:c.4922+3625G>A NP_001292353.1:n.4922+3625G>A
NM_020066.4:c.4910+3625G>A NP_064450.3:n.4910+3625G>A
NM_001348094.1:c.2738+3625G>A NP_001335023.1:n.2738+3625G>A
XM_017001840.2:c.3050+3625G>A XP_016857329.1:n.3050+3625G>A
XM_017001841.2:c.3050+3625G>A XP_016857330.1:n.3050+3625G>A
NM_020066.5:c.4910+3625G>A MANE Select NP_064450.3:n.4910+3625G>A
NM_001305424.2:c.4922+3625G>A NP_001292353.1:n.4922+3625G>A
NM_001348094.2:c.2738+3625G>A NP_001335023.1:n.2738+3625G>A