Canonical Allele Identifier: CA343456617

Gene: SDHC

Linked Data

• ClinVar Variation Id: 1021759
• ClinVar RCV Id: RCV001321576 ; RCV003166865
• dbSNP Id: rs1672292051
• MyVariant Identifiers: chr1:g.161326584T>G (hg19) ; chr1:g.161356794T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161356794T>G , CM000663.2:g.161356794T>G	GRCh38
NC_000001.10:g.161326584T>G , CM000663.1:g.161326584T>G	GRCh37
NC_000001.9:g.159593208T>G	NCBI36
NG_012767.1:g.47419T>G , LRG_317:g.47419T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*360T>G	ENSP00000482902.2:n.*360T>G
ENST00000367975.7:c.359T>G MANE Select	ENSP00000356953.3:p.Leu120Arg
ENST00000342751.8:c.242-5535T>G	ENSP00000356952.3:n.242-5535T>G
ENST00000367975.6:c.359T>G	ENSP00000356953.2:p.Leu120Arg
ENST00000392169.6:c.200T>G	ENSP00000376009.2:p.Leu67Arg
ENST00000432287.6:c.257T>G	ENSP00000390558.2:p.Leu86Arg
ENST00000470743.4:c.457T>G
ENST00000504963.5:c.*182T>G	ENSP00000423929.1:n.*182T>G
ENST00000513009.5:c.140-5535T>G	ENSP00000423260.1:n.140-5535T>G
NM_001035511.1:c.242-5535T>G	NP_001030588.1:n.242-5535T>G
NM_001035512.1:c.257T>G	NP_001030589.1:p.Leu86Arg
NM_001035513.1:c.200T>G	NP_001030590.1:p.Leu67Arg
NM_001278172.1:c.140-5535T>G	NP_001265101.1:n.140-5535T>G
NM_003001.3:c.359T>G , LRG_317t1:c.359T>G	NP_002992.1:p.Leu120Arg
NR_103459.1:n.416T>G
NM_001035511.2:c.242-5535T>G	NP_001030588.1:n.242-5535T>G
NM_001035512.2:c.257T>G	NP_001030589.1:p.Leu86Arg
NM_001035513.2:c.200T>G	NP_001030590.1:p.Leu67Arg
NM_001278172.2:c.140-5535T>G	NP_001265101.1:n.140-5535T>G
NM_003001.5:c.359T>G MANE Select	NP_002992.1:p.Leu120Arg
NR_103459.2:n.411T>G