Canonical Allele Identifier: CA678947458

Gene: SDHAF2

Linked Data

• dbSNP Id: rs1288788543
• gnomAD v3: 11-61437961-A-G
• gnomAD v4: 11-61437961-A-G
• MyVariant Identifiers: chr11:g.61205433A>G (hg19) ; chr11:g.61437961A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61437961A>G , CM000673.2:g.61437961A>G	GRCh38
NC_000011.9:g.61205433A>G , CM000673.1:g.61205433A>G	GRCh37
NC_000011.8:g.60962009A>G	NCBI36
NG_023393.1:g.12837A>G , LRG_519:g.12837A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.261-43A>G MANE Select	ENSP00000301761.3:n.261-43A>G
ENST00000301761.6:c.261-43A>G	ENSP00000301761.2:n.261-43A>G
ENST00000359614.9:c.261-43A>G	ENSP00000352630.5:n.261-43A>G
ENST00000534878.5:c.261-43A>G	ENSP00000471030.1:n.261-43A>G
ENST00000536250.1:c.*263-43A>G	ENSP00000471120.1:n.*263-43A>G
ENST00000536670.5:n.287-43A>G
ENST00000537782.5:c.261-43A>G	ENSP00000469951.1:n.261-43A>G
ENST00000538594.5:c.261-43A>G	ENSP00000440939.1:n.261-43A>G
ENST00000541135.5:c.261-43A>G	ENSP00000443130.1:n.261-43A>G
ENST00000542074.1:c.36+7779A>G	ENSP00000469670.1:n.36+7779A>G
ENST00000542794.5:c.*263-43A>G	ENSP00000439983.1:n.*263-43A>G
ENST00000543044.2:c.225-43A>G	ENSP00000440219.1:n.225-43A>G
ENST00000543265.1:c.260+113A>G	ENSP00000443660.1:n.260+113A>G
ENST00000544025.5:n.356-43A>G
ENST00000544801.5:c.261-43A>G	ENSP00000442581.1:n.261-43A>G
ENST00000544880.1:n.265-43A>G
NM_017841.2:c.261-43A>G , LRG_519t1:c.261-43A>G	NP_060311.1:n.261-43A>G
NM_017841.4:c.261-43A>G MANE Select	NP_060311.1:n.261-43A>G