Canonical Allele Identifier: CA343354908

Gene: SDHC

Linked Data

• ClinVar Variation Id: 465977
• ClinVar RCV Id: RCV000542616 ; RCV003159828 ; RCV003476281
• dbSNP Id: rs1198315342
• MyVariant Identifiers: chr1:g.161284199G>A (hg19) ; chr1:g.161314409G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161314409G>A , CM000663.2:g.161314409G>A	GRCh38
NC_000001.10:g.161284199G>A , CM000663.1:g.161284199G>A	GRCh37
NC_000001.9:g.159550823G>A	NCBI36
NG_008055.1:g.564C>T , LRG_256:g.564C>T
NG_012767.1:g.5034G>A , LRG_317:g.5034G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.4G>A	ENSP00000482902.2:p.Ala2Thr
ENST00000367975.7:c.4G>A MANE Select	ENSP00000356953.3:p.Ala2Thr
ENST00000342751.8:c.4G>A	ENSP00000356952.3:p.Ala2Thr
ENST00000367975.6:c.4G>A	ENSP00000356953.2:p.Ala2Thr
ENST00000392169.6:c.4G>A	ENSP00000376009.2:p.Ala2Thr
ENST00000432287.6:c.4G>A	ENSP00000390558.2:p.Ala2Thr
ENST00000504963.5:c.4G>A	ENSP00000423929.1:p.Ala2Thr
ENST00000513009.5:c.4G>A	ENSP00000423260.1:p.Ala2Thr
ENST00000515731.1:n.29G>A
NM_001035511.1:c.4G>A	NP_001030588.1:p.Ala2Thr
NM_001035512.1:c.4G>A	NP_001030589.1:p.Ala2Thr
NM_001035513.1:c.4G>A	NP_001030590.1:p.Ala2Thr
NM_001278172.1:c.4G>A	NP_001265101.1:p.Ala2Thr
NM_003001.3:c.4G>A , LRG_317t1:c.4G>A	NP_002992.1:p.Ala2Thr
NR_103459.1:n.34G>A
NM_001035511.2:c.4G>A	NP_001030588.1:p.Ala2Thr
NM_001035512.2:c.4G>A	NP_001030589.1:p.Ala2Thr
NM_001035513.2:c.4G>A	NP_001030590.1:p.Ala2Thr
NM_001278172.2:c.4G>A	NP_001265101.1:p.Ala2Thr
NM_003001.5:c.4G>A MANE Select	NP_002992.1:p.Ala2Thr
NR_103459.2:n.29G>A