Canonical Allele Identifier: CA222882531
Gene: SDHAF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1415598
dbSNP Id: rs1056273933

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446024A>G , CM000673.2:g.61446024A>G GRCh38
NC_000011.9:g.61213496A>G , CM000673.1:g.61213496A>G GRCh37
NC_000011.8:g.60970072A>G NCBI36
NG_023393.1:g.20900A>G , LRG_519:g.20900A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.454A>G MANE Select ENSP00000301761.3:p.Arg152Gly
ENST00000301761.6:c.454A>G ENSP00000301761.2:p.Arg152Gly
ENST00000536670.5:n.396+7911A>G
ENST00000537782.5:c.*100A>G ENSP00000469951.1:n.*100A>G
ENST00000538594.5:c.370+7911A>G ENSP00000440939.1:n.370+7911A>G
ENST00000541135.5:c.377+7904A>G ENSP00000443130.1:n.377+7904A>G
ENST00000542074.1:c.*33A>G ENSP00000469670.1:n.*33A>G
ENST00000542794.5:c.*456A>G ENSP00000439983.1:n.*456A>G
ENST00000543044.2:c.418A>G ENSP00000440219.1:p.Arg140Gly
ENST00000543265.1:c.*77A>G ENSP00000443660.1:n.*77A>G
ENST00000544025.5:n.465+7911A>G
ENST00000544801.5:c.370+7911A>G ENSP00000442581.1:n.370+7911A>G
ENST00000544880.1:n.374+7911A>G
NM_017841.2:c.454A>G , LRG_519t1:c.454A>G NP_060311.1:p.Arg152Gly
NM_017841.4:c.454A>G MANE Select NP_060311.1:p.Arg152Gly