Canonical Allele Identifier: CA2613847620

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446249-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446249C>G , CM000673.2:g.61446249C>G	GRCh38
NC_000011.9:g.61213721C>G , CM000673.1:g.61213721C>G	GRCh37
NC_000011.8:g.60970297C>G	NCBI36
NG_023393.1:g.21125C>G , LRG_519:g.21125C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*178C>G MANE Select	ENSP00000301761.3:n.*178C>G
ENST00000301761.6:c.*178C>G	ENSP00000301761.2:n.*178C>G
ENST00000536670.5:n.396+8136C>G
ENST00000538594.5:c.370+8136C>G	ENSP00000440939.1:n.370+8136C>G
ENST00000541135.5:c.377+8129C>G	ENSP00000443130.1:n.377+8129C>G
ENST00000542074.1:c.*258C>G	ENSP00000469670.1:n.*258C>G
ENST00000542794.5:c.*681C>G	ENSP00000439983.1:n.*681C>G
ENST00000543044.2:c.*160+18C>G	ENSP00000440219.1:n.*160+18C>G
ENST00000544025.5:n.465+8136C>G
ENST00000544801.5:c.370+8136C>G	ENSP00000442581.1:n.370+8136C>G
ENST00000544880.1:n.374+8136C>G
NM_017841.2:c.*178C>G , LRG_519t1:c.*178C>G	NP_060311.1:n.*178C>G
NM_017841.4:c.*178C>G MANE Select	NP_060311.1:n.*178C>G