Canonical Allele Identifier: CA2613847977

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446504-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446504T>G , CM000673.2:g.61446504T>G	GRCh38
NC_000011.9:g.61213976T>G , CM000673.1:g.61213976T>G	GRCh37
NC_000011.8:g.60970552T>G	NCBI36
NG_023393.1:g.21380T>G , LRG_519:g.21380T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*433T>G MANE Select	ENSP00000301761.3:n.*433T>G
ENST00000301761.6:c.*433T>G	ENSP00000301761.2:n.*433T>G
ENST00000536670.5:n.396+8391T>G
ENST00000538594.5:c.370+8391T>G	ENSP00000440939.1:n.370+8391T>G
ENST00000541135.5:c.377+8384T>G	ENSP00000443130.1:n.377+8384T>G
ENST00000542074.1:c.*513T>G	ENSP00000469670.1:n.*513T>G
ENST00000543044.2:c.*160+273T>G	ENSP00000440219.1:n.*160+273T>G
ENST00000544025.5:n.465+8391T>G
ENST00000544801.5:c.370+8391T>G	ENSP00000442581.1:n.370+8391T>G
ENST00000544880.1:n.374+8391T>G
NM_017841.2:c.*433T>G , LRG_519t1:c.*433T>G	NP_060311.1:n.*433T>G
NM_017841.4:c.*433T>G MANE Select	NP_060311.1:n.*433T>G