Canonical Allele Identifier: CA343456768
Gene: SDHC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161356837C>A , CM000663.2:g.161356837C>A GRCh38
NC_000001.10:g.161326627C>A , CM000663.1:g.161326627C>A GRCh37
NC_000001.9:g.159593251C>A NCBI36
NG_012767.1:g.47462C>A , LRG_317:g.47462C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000470743.5:c.*403C>A ENSP00000482902.2:n.*403C>A
ENST00000367975.7:c.402C>A MANE Select ENSP00000356953.3:p.His134Gln
ENST00000342751.8:c.242-5492C>A ENSP00000356952.3:n.242-5492C>A
ENST00000367975.6:c.402C>A ENSP00000356953.2:p.His134Gln
ENST00000392169.6:c.243C>A ENSP00000376009.2:p.His81Gln
ENST00000432287.6:c.300C>A ENSP00000390558.2:p.His100Gln
ENST00000470743.4:c.500C>A
ENST00000504963.5:c.*225C>A ENSP00000423929.1:n.*225C>A
ENST00000513009.5:c.140-5492C>A ENSP00000423260.1:n.140-5492C>A
NM_001035511.1:c.242-5492C>A NP_001030588.1:n.242-5492C>A
NM_001035512.1:c.300C>A NP_001030589.1:p.His100Gln
NM_001035513.1:c.243C>A NP_001030590.1:p.His81Gln
NM_001278172.1:c.140-5492C>A NP_001265101.1:n.140-5492C>A
NM_003001.3:c.402C>A , LRG_317t1:c.402C>A NP_002992.1:p.His134Gln
NR_103459.1:n.459C>A
NM_001035511.2:c.242-5492C>A NP_001030588.1:n.242-5492C>A
NM_001035512.2:c.300C>A NP_001030589.1:p.His100Gln
NM_001035513.2:c.243C>A NP_001030590.1:p.His81Gln
NM_001278172.2:c.140-5492C>A NP_001265101.1:n.140-5492C>A
NM_003001.5:c.402C>A MANE Select NP_002992.1:p.His134Gln
NR_103459.2:n.454C>A