Canonical Allele Identifier: CA343360831

Gene: SDHC

Linked Data

• ClinVar Variation Id: 938758
• ClinVar RCV Id: RCV001208039 ; RCV002509630
• dbSNP Id: rs754818119
• MyVariant Identifiers: chr1:g.161298190G>C (hg19) ; chr1:g.161328400G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161328400G>C , CM000663.2:g.161328400G>C	GRCh38
NC_000001.10:g.161298190G>C , CM000663.1:g.161298190G>C	GRCh37
NC_000001.9:g.159564814G>C	NCBI36
NG_012767.1:g.19025G>C , LRG_317:g.19025G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*83G>C	ENSP00000482902.2:n.*83G>C
ENST00000367975.7:c.82G>C MANE Select	ENSP00000356953.3:p.Val28Leu
ENST00000342751.8:c.82G>C	ENSP00000356952.3:p.Val28Leu
ENST00000367975.6:c.82G>C	ENSP00000356953.2:p.Val28Leu
ENST00000392169.6:c.21-12194G>C	ENSP00000376009.2:n.21-12194G>C
ENST00000432287.6:c.77+4730G>C	ENSP00000390558.2:n.77+4730G>C
ENST00000470743.4:c.180G>C
ENST00000504963.5:c.82G>C	ENSP00000423929.1:p.Val28Leu
ENST00000513009.5:c.77+4730G>C	ENSP00000423260.1:n.77+4730G>C
ENST00000515731.1:n.556G>C
NM_001035511.1:c.82G>C	NP_001030588.1:p.Val28Leu
NM_001035512.1:c.77+4730G>C	NP_001030589.1:n.77+4730G>C
NM_001035513.1:c.21-12194G>C	NP_001030590.1:n.21-12194G>C
NM_001278172.1:c.77+4730G>C	NP_001265101.1:n.77+4730G>C
NM_003001.3:c.82G>C , LRG_317t1:c.82G>C	NP_002992.1:p.Val28Leu
NR_103459.1:n.112G>C
NM_001035511.2:c.82G>C	NP_001030588.1:p.Val28Leu
NM_001035512.2:c.77+4730G>C	NP_001030589.1:n.77+4730G>C
NM_001035513.2:c.21-12194G>C	NP_001030590.1:n.21-12194G>C
NM_001278172.2:c.77+4730G>C	NP_001265101.1:n.77+4730G>C
NM_003001.5:c.82G>C MANE Select	NP_002992.1:p.Val28Leu
NR_103459.2:n.107G>C