Canonical Allele Identifier: CA10827741
Gene: FMN2 HGNC NCBI

Linked Data

dbSNP Id: rs17672135

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240282296T>C , CM000663.2:g.240282296T>C GRCh38
NC_000001.10:g.240445596T>C , CM000663.1:g.240445596T>C GRCh37
NC_000001.9:g.238512219T>C NCBI36
NG_042054.1:g.195412T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000319653.14:c.4154-12526T>C MANE Select ENSP00000318884.9:n.4154-12526T>C
ENST00000545751.3:c.57-46780T>C
ENST00000679390.1:n.416-12526T>C
ENST00000679980.1:c.423-12526T>C
ENST00000681131.1:c.81-12526T>C
ENST00000681210.1:c.374-12526T>C ENSP00000505131.1:n.374-12526T>C
ENST00000681741.1:c.*198-12526T>C ENSP00000505116.1:n.*198-12526T>C
ENST00000681805.1:c.39-12526T>C
ENST00000681824.1:c.374-12526T>C ENSP00000505818.1:n.374-12526T>C
ENST00000319653.13:c.4154-12526T>C ENSP00000318884.9:n.4154-12526T>C
ENST00000441342.1:c.92-12526T>C ENSP00000388922.1:n.92-12526T>C
ENST00000463398.5:n.214-12526T>C
NM_001305424.1:c.4166-12526T>C NP_001292353.1:n.4166-12526T>C
NM_020066.4:c.4154-12526T>C NP_064450.3:n.4154-12526T>C
NM_001348094.1:c.2075-12526T>C NP_001335023.1:n.2075-12526T>C
XM_017001837.1:c.4166-12526T>C XP_016857326.1:n.4166-12526T>C
XM_017001840.2:c.2294-12526T>C XP_016857329.1:n.2294-12526T>C
XM_017001841.2:c.2294-12526T>C XP_016857330.1:n.2294-12526T>C
NM_020066.5:c.4154-12526T>C MANE Select NP_064450.3:n.4154-12526T>C
NM_001305424.2:c.4166-12526T>C NP_001292353.1:n.4166-12526T>C
NM_001348094.2:c.2075-12526T>C NP_001335023.1:n.2075-12526T>C