Canonical Allele Identifier: CA10638835
Gene: SDHAF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 305096
ClinVar RCV Id: RCV000314128
dbSNP Id: rs886048416

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446184C>A , CM000673.2:g.61446184C>A GRCh38
NC_000011.9:g.61213656C>A , CM000673.1:g.61213656C>A GRCh37
NC_000011.8:g.60970232C>A NCBI36
NG_023393.1:g.21060C>A , LRG_519:g.21060C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301761.7:c.*113C>A MANE Select ENSP00000301761.3:n.*113C>A
ENST00000301761.6:c.*113C>A ENSP00000301761.2:n.*113C>A
ENST00000536670.5:n.396+8071C>A
ENST00000538594.5:c.370+8071C>A ENSP00000440939.1:n.370+8071C>A
ENST00000541135.5:c.377+8064C>A ENSP00000443130.1:n.377+8064C>A
ENST00000542074.1:c.*193C>A ENSP00000469670.1:n.*193C>A
ENST00000542794.5:c.*616C>A ENSP00000439983.1:n.*616C>A
ENST00000543044.2:c.*113C>A ENSP00000440219.1:n.*113C>A
ENST00000544025.5:n.465+8071C>A
ENST00000544801.5:c.370+8071C>A ENSP00000442581.1:n.370+8071C>A
ENST00000544880.1:n.374+8071C>A
NM_017841.2:c.*113C>A , LRG_519t1:c.*113C>A NP_060311.1:n.*113C>A
NM_017841.4:c.*113C>A MANE Select NP_060311.1:n.*113C>A