Canonical Allele Identifier: CA1977301539

Gene: SDHAF2

Linked Data

• dbSNP Id: rs1862139838
• gnomAD v4: 11-61446455-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446455C>G , CM000673.2:g.61446455C>G	GRCh38
NC_000011.9:g.61213927C>G , CM000673.1:g.61213927C>G	GRCh37
NC_000011.8:g.60970503C>G	NCBI36
NG_023393.1:g.21331C>G , LRG_519:g.21331C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*384C>G MANE Select	ENSP00000301761.3:n.*384C>G
ENST00000301761.6:c.*384C>G	ENSP00000301761.2:n.*384C>G
ENST00000536670.5:n.396+8342C>G
ENST00000538594.5:c.370+8342C>G	ENSP00000440939.1:n.370+8342C>G
ENST00000541135.5:c.377+8335C>G	ENSP00000443130.1:n.377+8335C>G
ENST00000542074.1:c.*464C>G	ENSP00000469670.1:n.*464C>G
ENST00000543044.2:c.*160+224C>G	ENSP00000440219.1:n.*160+224C>G
ENST00000544025.5:n.465+8342C>G
ENST00000544801.5:c.370+8342C>G	ENSP00000442581.1:n.370+8342C>G
ENST00000544880.1:n.374+8342C>G
NM_017841.2:c.*384C>G , LRG_519t1:c.*384C>G	NP_060311.1:n.*384C>G
NM_017841.4:c.*384C>G MANE Select	NP_060311.1:n.*384C>G