Canonical Allele Identifier: CA2613847590

Gene: SDHAF2

Linked Data

• dbSNP Id: rs1862136651
• gnomAD v4: 11-61446233-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446233T>A , CM000673.2:g.61446233T>A	GRCh38
NC_000011.9:g.61213705T>A , CM000673.1:g.61213705T>A	GRCh37
NC_000011.8:g.60970281T>A	NCBI36
NG_023393.1:g.21109T>A , LRG_519:g.21109T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*162T>A MANE Select	ENSP00000301761.3:n.*162T>A
ENST00000301761.6:c.*162T>A	ENSP00000301761.2:n.*162T>A
ENST00000536670.5:n.396+8120T>A
ENST00000538594.5:c.370+8120T>A	ENSP00000440939.1:n.370+8120T>A
ENST00000541135.5:c.377+8113T>A	ENSP00000443130.1:n.377+8113T>A
ENST00000542074.1:c.*242T>A	ENSP00000469670.1:n.*242T>A
ENST00000542794.5:c.*665T>A	ENSP00000439983.1:n.*665T>A
ENST00000543044.2:c.*160+2T>A	ENSP00000440219.1:n.*160+2T>A
ENST00000544025.5:n.465+8120T>A
ENST00000544801.5:c.370+8120T>A	ENSP00000442581.1:n.370+8120T>A
ENST00000544880.1:n.374+8120T>A
NM_017841.2:c.*162T>A , LRG_519t1:c.*162T>A	NP_060311.1:n.*162T>A
NM_017841.4:c.*162T>A MANE Select	NP_060311.1:n.*162T>A