Canonical Allele Identifier: CA058271

Gene: SDHAF2

Linked Data

• dbSNP Id: rs550980414
• ExAC: 11:61205435 C / A
• gnomAD v2: 11-61205435-C-A
• gnomAD v3: 11-61437963-C-A
• gnomAD v4: 11-61437963-C-A
• MyVariant Identifiers: chr11:g.61205435C>A (hg19) ; chr11:g.61437963C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61437963C>A , CM000673.2:g.61437963C>A	GRCh38
NC_000011.9:g.61205435C>A , CM000673.1:g.61205435C>A	GRCh37
NC_000011.8:g.60962011C>A	NCBI36
NG_023393.1:g.12839C>A , LRG_519:g.12839C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.261-41C>A MANE Select	ENSP00000301761.3:n.261-41C>A
ENST00000301761.6:c.261-41C>A	ENSP00000301761.2:n.261-41C>A
ENST00000359614.9:c.261-41C>A	ENSP00000352630.5:n.261-41C>A
ENST00000534878.5:c.261-41C>A	ENSP00000471030.1:n.261-41C>A
ENST00000536250.1:c.*263-41C>A	ENSP00000471120.1:n.*263-41C>A
ENST00000536670.5:n.287-41C>A
ENST00000537782.5:c.261-41C>A	ENSP00000469951.1:n.261-41C>A
ENST00000538594.5:c.261-41C>A	ENSP00000440939.1:n.261-41C>A
ENST00000541135.5:c.261-41C>A	ENSP00000443130.1:n.261-41C>A
ENST00000542074.1:c.36+7781C>A	ENSP00000469670.1:n.36+7781C>A
ENST00000542794.5:c.*263-41C>A	ENSP00000439983.1:n.*263-41C>A
ENST00000543044.2:c.225-41C>A	ENSP00000440219.1:n.225-41C>A
ENST00000543265.1:c.260+115C>A	ENSP00000443660.1:n.260+115C>A
ENST00000544025.5:n.356-41C>A
ENST00000544801.5:c.261-41C>A	ENSP00000442581.1:n.261-41C>A
ENST00000544880.1:n.265-41C>A
NM_017841.2:c.261-41C>A , LRG_519t1:c.261-41C>A	NP_060311.1:n.261-41C>A
NM_017841.4:c.261-41C>A MANE Select	NP_060311.1:n.261-41C>A