Canonical Allele Identifier: CA2597657668

Gene: SDHAF2

Linked Data

• dbSNP Id: rs2134902264
• gnomAD v3: 11-61446095-G-A
• gnomAD v4: 11-61446095-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446095G>A , CM000673.2:g.61446095G>A	GRCh38
NC_000011.9:g.61213567G>A , CM000673.1:g.61213567G>A	GRCh37
NC_000011.8:g.60970143G>A	NCBI36
NG_023393.1:g.20971G>A , LRG_519:g.20971G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000301761.7:c.*24G>A MANE Select	ENSP00000301761.3:n.*24G>A
ENST00000301761.6:c.*24G>A	ENSP00000301761.2:n.*24G>A
ENST00000536670.5:n.396+7982G>A
ENST00000538594.5:c.370+7982G>A	ENSP00000440939.1:n.370+7982G>A
ENST00000541135.5:c.377+7975G>A	ENSP00000443130.1:n.377+7975G>A
ENST00000542074.1:c.*104G>A	ENSP00000469670.1:n.*104G>A
ENST00000542794.5:c.*527G>A	ENSP00000439983.1:n.*527G>A
ENST00000543044.2:c.*24G>A	ENSP00000440219.1:n.*24G>A
ENST00000543265.1:c.*148G>A	ENSP00000443660.1:n.*148G>A
ENST00000544025.5:n.465+7982G>A
ENST00000544801.5:c.370+7982G>A	ENSP00000442581.1:n.370+7982G>A
ENST00000544880.1:n.374+7982G>A
NM_017841.2:c.*24G>A , LRG_519t1:c.*24G>A	NP_060311.1:n.*24G>A
NM_017841.4:c.*24G>A MANE Select	NP_060311.1:n.*24G>A