Canonical Allele Identifier: CA2613847382
Gene: SDHAF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446116A>G , CM000673.2:g.61446116A>G GRCh38
NC_000011.9:g.61213588A>G , CM000673.1:g.61213588A>G GRCh37
NC_000011.8:g.60970164A>G NCBI36
NG_023393.1:g.20992A>G , LRG_519:g.20992A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301761.7:c.*45A>G MANE Select ENSP00000301761.3:n.*45A>G
ENST00000301761.6:c.*45A>G ENSP00000301761.2:n.*45A>G
ENST00000536670.5:n.396+8003A>G
ENST00000538594.5:c.370+8003A>G ENSP00000440939.1:n.370+8003A>G
ENST00000541135.5:c.377+7996A>G ENSP00000443130.1:n.377+7996A>G
ENST00000542074.1:c.*125A>G ENSP00000469670.1:n.*125A>G
ENST00000542794.5:c.*548A>G ENSP00000439983.1:n.*548A>G
ENST00000543044.2:c.*45A>G ENSP00000440219.1:n.*45A>G
ENST00000544025.5:n.465+8003A>G
ENST00000544801.5:c.370+8003A>G ENSP00000442581.1:n.370+8003A>G
ENST00000544880.1:n.374+8003A>G
NM_017841.2:c.*45A>G , LRG_519t1:c.*45A>G NP_060311.1:n.*45A>G
NM_017841.4:c.*45A>G MANE Select NP_060311.1:n.*45A>G