Canonical Allele Identifier: CA15099728
Gene: FMN2 HGNC NCBI

Linked Data

dbSNP Id: rs11810574

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240120436A>G , CM000663.2:g.240120436A>G GRCh38
NC_000001.10:g.240283736A>G , CM000663.1:g.240283736A>G GRCh37
NC_000001.9:g.238350359A>G NCBI36
NG_042054.1:g.33552A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000319653.14:c.1616-2743A>G MANE Select ENSP00000318884.9:n.1616-2743A>G
ENST00000319653.13:c.1616-2743A>G ENSP00000318884.9:n.1616-2743A>G
ENST00000447095.5:c.-86-2743A>G ENSP00000409308.1:n.-86-2743A>G
NM_001305424.1:c.1616-2743A>G NP_001292353.1:n.1616-2743A>G
NM_020066.4:c.1616-2743A>G NP_064450.3:n.1616-2743A>G
XM_011544237.1:c.1616-2743A>G XP_011542539.1:n.1616-2743A>G
XR_949151.1:n.1837-2743A>G
NM_001348094.1:c.1616-2743A>G NP_001335023.1:n.1616-2743A>G
XM_011544237.3:c.1616-2743A>G XP_011542539.1:n.1616-2743A>G
XM_017001837.1:c.1616-2743A>G XP_016857326.1:n.1616-2743A>G
XM_017001838.1:c.1616-2743A>G XP_016857327.1:n.1616-2743A>G
NM_020066.5:c.1616-2743A>G MANE Select NP_064450.3:n.1616-2743A>G
NM_001305424.2:c.1616-2743A>G NP_001292353.1:n.1616-2743A>G
NM_001348094.2:c.1616-2743A>G NP_001335023.1:n.1616-2743A>G