Canonical Allele Identifier: CA678946526

Gene: SDHAF2

Linked Data

• dbSNP Id: rs1421156976
• gnomAD v4: 11-61446476-C-A
• MyVariant Identifiers: chr11:g.61213948C>A (hg19) ; chr11:g.61446476C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446476C>A , CM000673.2:g.61446476C>A	GRCh38
NC_000011.9:g.61213948C>A , CM000673.1:g.61213948C>A	GRCh37
NC_000011.8:g.60970524C>A	NCBI36
NG_023393.1:g.21352C>A , LRG_519:g.21352C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*405C>A MANE Select	ENSP00000301761.3:n.*405C>A
ENST00000301761.6:c.*405C>A	ENSP00000301761.2:n.*405C>A
ENST00000536670.5:n.396+8363C>A
ENST00000538594.5:c.370+8363C>A	ENSP00000440939.1:n.370+8363C>A
ENST00000541135.5:c.377+8356C>A	ENSP00000443130.1:n.377+8356C>A
ENST00000542074.1:c.*485C>A	ENSP00000469670.1:n.*485C>A
ENST00000543044.2:c.*160+245C>A	ENSP00000440219.1:n.*160+245C>A
ENST00000544025.5:n.465+8363C>A
ENST00000544801.5:c.370+8363C>A	ENSP00000442581.1:n.370+8363C>A
ENST00000544880.1:n.374+8363C>A
NM_017841.2:c.*405C>A , LRG_519t1:c.*405C>A	NP_060311.1:n.*405C>A
NM_017841.4:c.*405C>A MANE Select	NP_060311.1:n.*405C>A