Canonical Allele Identifier: CA1977301146

Gene: SDHAF2

Linked Data

• dbSNP Id: rs1862134146

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446073C>G , CM000673.2:g.61446073C>G	GRCh38
NC_000011.9:g.61213545C>G , CM000673.1:g.61213545C>G	GRCh37
NC_000011.8:g.60970121C>G	NCBI36
NG_023393.1:g.20949C>G , LRG_519:g.20949C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*2C>G MANE Select	ENSP00000301761.3:n.*2C>G
ENST00000301761.6:c.*2C>G	ENSP00000301761.2:n.*2C>G
ENST00000536670.5:n.396+7960C>G
ENST00000538594.5:c.370+7960C>G	ENSP00000440939.1:n.370+7960C>G
ENST00000541135.5:c.377+7953C>G	ENSP00000443130.1:n.377+7953C>G
ENST00000542074.1:c.*82C>G	ENSP00000469670.1:n.*82C>G
ENST00000542794.5:c.*505C>G	ENSP00000439983.1:n.*505C>G
ENST00000543044.2:c.*2C>G	ENSP00000440219.1:n.*2C>G
ENST00000543265.1:c.*126C>G	ENSP00000443660.1:n.*126C>G
ENST00000544025.5:n.465+7960C>G
ENST00000544801.5:c.370+7960C>G	ENSP00000442581.1:n.370+7960C>G
ENST00000544880.1:n.374+7960C>G
NM_017841.2:c.*2C>G , LRG_519t1:c.*2C>G	NP_060311.1:n.*2C>G
NM_017841.4:c.*2C>G MANE Select	NP_060311.1:n.*2C>G