Canonical Allele Identifier: CA1977301128
Gene: SDHAF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446067G= , CM000673.2:g.61446067G= GRCh38
NC_000011.9:g.61213539G= , CM000673.1:g.61213539G= GRCh37
NC_000011.8:g.60970115G= NCBI36
NG_023393.1:g.20943G= , LRG_519:g.20943G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.497G= MANE Select ENSP00000301761.3:p.Arg166=
ENST00000301761.6:c.497G= ENSP00000301761.2:p.Arg166=
ENST00000536670.5:n.396+7954G=
ENST00000538594.5:c.370+7954G= ENSP00000440939.1:n.370+7954G=
ENST00000541135.5:c.377+7947G= ENSP00000443130.1:n.377+7947G=
ENST00000542074.1:c.*76G= ENSP00000469670.1:n.*76G=
ENST00000542794.5:c.*499G= ENSP00000439983.1:n.*499G=
ENST00000543044.2:c.461G= ENSP00000440219.1:p.Arg154=
ENST00000543265.1:c.*120G= ENSP00000443660.1:n.*120G=
ENST00000544025.5:n.465+7954G=
ENST00000544801.5:c.370+7954G= ENSP00000442581.1:n.370+7954G=
ENST00000544880.1:n.374+7954G=
NM_017841.2:c.497G= , LRG_519t1:c.497G= NP_060311.1:p.Arg166=
NM_017841.4:c.497G= MANE Select NP_060311.1:p.Arg166=