Canonical Allele Identifier: CA678946532

Gene: SDHAF2

Linked Data

• dbSNP Id: rs1238686473
• gnomAD v3: 11-61446495-G-A
• gnomAD v4: 11-61446495-G-A
• MyVariant Identifiers: chr11:g.61213967G>A (hg19) ; chr11:g.61446495G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446495G>A , CM000673.2:g.61446495G>A	GRCh38
NC_000011.9:g.61213967G>A , CM000673.1:g.61213967G>A	GRCh37
NC_000011.8:g.60970543G>A	NCBI36
NG_023393.1:g.21371G>A , LRG_519:g.21371G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*424G>A MANE Select	ENSP00000301761.3:n.*424G>A
ENST00000301761.6:c.*424G>A	ENSP00000301761.2:n.*424G>A
ENST00000536670.5:n.396+8382G>A
ENST00000538594.5:c.370+8382G>A	ENSP00000440939.1:n.370+8382G>A
ENST00000541135.5:c.377+8375G>A	ENSP00000443130.1:n.377+8375G>A
ENST00000542074.1:c.*504G>A	ENSP00000469670.1:n.*504G>A
ENST00000543044.2:c.*160+264G>A	ENSP00000440219.1:n.*160+264G>A
ENST00000544025.5:n.465+8382G>A
ENST00000544801.5:c.370+8382G>A	ENSP00000442581.1:n.370+8382G>A
ENST00000544880.1:n.374+8382G>A
NM_017841.2:c.*424G>A , LRG_519t1:c.*424G>A	NP_060311.1:n.*424G>A
NM_017841.4:c.*424G>A MANE Select	NP_060311.1:n.*424G>A