Canonical Allele Identifier: CA058016

Gene: SDHAF2

Linked Data

• dbSNP Id: rs767772474
• ExAC: 11:61213565 T / G
• gnomAD v2: 11-61213565-T-G
• gnomAD v4: 11-61446093-T-G
• MyVariant Identifiers: chr11:g.61213565T>G (hg19) ; chr11:g.61446093T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446093T>G , CM000673.2:g.61446093T>G	GRCh38
NC_000011.9:g.61213565T>G , CM000673.1:g.61213565T>G	GRCh37
NC_000011.8:g.60970141T>G	NCBI36
NG_023393.1:g.20969T>G , LRG_519:g.20969T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000301761.7:c.*22T>G MANE Select	ENSP00000301761.3:n.*22T>G
ENST00000301761.6:c.*22T>G	ENSP00000301761.2:n.*22T>G
ENST00000536670.5:n.396+7980T>G
ENST00000538594.5:c.370+7980T>G	ENSP00000440939.1:n.370+7980T>G
ENST00000541135.5:c.377+7973T>G	ENSP00000443130.1:n.377+7973T>G
ENST00000542074.1:c.*102T>G	ENSP00000469670.1:n.*102T>G
ENST00000542794.5:c.*525T>G	ENSP00000439983.1:n.*525T>G
ENST00000543044.2:c.*22T>G	ENSP00000440219.1:n.*22T>G
ENST00000543265.1:c.*146T>G	ENSP00000443660.1:n.*146T>G
ENST00000544025.5:n.465+7980T>G
ENST00000544801.5:c.370+7980T>G	ENSP00000442581.1:n.370+7980T>G
ENST00000544880.1:n.374+7980T>G
NM_017841.2:c.*22T>G , LRG_519t1:c.*22T>G	NP_060311.1:n.*22T>G
NM_017841.4:c.*22T>G MANE Select	NP_060311.1:n.*22T>G