Canonical Allele Identifier: CA9191361
Gene: FDX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10315921T>C , CM000681.2:g.10315921T>C GRCh38
NC_000019.9:g.10426597T>C , CM000681.1:g.10426597T>C GRCh37
NC_000019.8:g.10287597T>C NCBI36
NG_034259.1:g.5095A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706663.1:c.51+25A>G ENSP00000516489.1:n.51+25A>G
ENST00000343376.8:n.93A>G
ENST00000393708.3:c.85A>G MANE Select ENSP00000377311.4:p.Arg29Gly
ENST00000452032.6:c.85A>G ENSP00000408510.2:p.Arg29Gly
ENST00000453681.1:n.90A>G
ENST00000460631.5:n.76A>G
ENST00000486454.1:n.86A>G
ENST00000494368.5:c.-261+49A>G ENSP00000467188.1:n.-261+49A>G
ENST00000586529.1:c.1773+97A>G ENSP00000467814.1:n.1773+97A>G
NM_001031734.3:c.85A>G NP_001026904.2:p.Arg29Gly
NM_001031734.4:c.85A>G NP_001026904.2:p.Arg29Gly
NM_001397406.1:c.76A>G MANE Select NP_001384335.1:p.Arg26Gly