Canonical Allele Identifier: CA2574841569

Gene: SDHAF2

Linked Data

• dbSNP Id: rs2134902215

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446078C>T , CM000673.2:g.61446078C>T	GRCh38
NC_000011.9:g.61213550C>T , CM000673.1:g.61213550C>T	GRCh37
NC_000011.8:g.60970126C>T	NCBI36
NG_023393.1:g.20954C>T , LRG_519:g.20954C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*7C>T MANE Select	ENSP00000301761.3:n.*7C>T
ENST00000301761.6:c.*7C>T	ENSP00000301761.2:n.*7C>T
ENST00000536670.5:n.396+7965C>T
ENST00000538594.5:c.370+7965C>T	ENSP00000440939.1:n.370+7965C>T
ENST00000541135.5:c.377+7958C>T	ENSP00000443130.1:n.377+7958C>T
ENST00000542074.1:c.*87C>T	ENSP00000469670.1:n.*87C>T
ENST00000542794.5:c.*510C>T	ENSP00000439983.1:n.*510C>T
ENST00000543044.2:c.*7C>T	ENSP00000440219.1:n.*7C>T
ENST00000543265.1:c.*131C>T	ENSP00000443660.1:n.*131C>T
ENST00000544025.5:n.465+7965C>T
ENST00000544801.5:c.370+7965C>T	ENSP00000442581.1:n.370+7965C>T
ENST00000544880.1:n.374+7965C>T
NM_017841.2:c.*7C>T , LRG_519t1:c.*7C>T	NP_060311.1:n.*7C>T
NM_017841.4:c.*7C>T MANE Select	NP_060311.1:n.*7C>T