Canonical Allele Identifier: CA222882668

Gene: SDHAF2

Linked Data

• dbSNP Id: rs866801707
• gnomAD v4: 11-61446176-C-T
• MyVariant Identifiers: chr11:g.61213648C>T (hg19) ; chr11:g.61446176C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446176C>T , CM000673.2:g.61446176C>T	GRCh38
NC_000011.9:g.61213648C>T , CM000673.1:g.61213648C>T	GRCh37
NC_000011.8:g.60970224C>T	NCBI36
NG_023393.1:g.21052C>T , LRG_519:g.21052C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*105C>T MANE Select	ENSP00000301761.3:n.*105C>T
ENST00000301761.6:c.*105C>T	ENSP00000301761.2:n.*105C>T
ENST00000536670.5:n.396+8063C>T
ENST00000538594.5:c.370+8063C>T	ENSP00000440939.1:n.370+8063C>T
ENST00000541135.5:c.377+8056C>T	ENSP00000443130.1:n.377+8056C>T
ENST00000542074.1:c.*185C>T	ENSP00000469670.1:n.*185C>T
ENST00000542794.5:c.*608C>T	ENSP00000439983.1:n.*608C>T
ENST00000543044.2:c.*105C>T	ENSP00000440219.1:n.*105C>T
ENST00000544025.5:n.465+8063C>T
ENST00000544801.5:c.370+8063C>T	ENSP00000442581.1:n.370+8063C>T
ENST00000544880.1:n.374+8063C>T
NM_017841.2:c.*105C>T , LRG_519t1:c.*105C>T	NP_060311.1:n.*105C>T
NM_017841.4:c.*105C>T MANE Select	NP_060311.1:n.*105C>T