Canonical Allele Identifier: CA10608582
Gene: SDHC HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.161363401A>G
GRCh37 chr1:g.161333191A>G
gnomAD v2:
1:161333191 A / G
gnomAD v3:
1:161363401 A / G
gnomAD v4:
chr1-161363401-A-G
Joint Max Group AF 0.26714103 (EAS)
Genomes Max Group AF 0.21242084 (AFR)
Exomes Max Group AF 0.2943269 (EAS)
ClinVar RCV:
RCV000268716
ClinVar Variation:
293337
dbSNP:
4600063
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161363401A>G , CM000663.2:g.161363401A>G GRCh38
NC_000001.10:g.161333191A>G , CM000663.1:g.161333191A>G GRCh37
NC_000001.9:g.159599815A>G NCBI36
NG_012767.1:g.54026A>G , LRG_317:g.54026A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367975.6:c.*968A>G ENSP00000356953.2:n.*968A>G
NM_001035511.1:c.*861A>G NP_001030588.1:n.*861A>G
NM_001035512.1:c.*968A>G NP_001030589.1:n.*968A>G
NM_001035513.1:c.*968A>G NP_001030590.1:n.*968A>G
NM_001278172.1:c.*861A>G NP_001265101.1:n.*861A>G
NM_003001.3:c.*968A>G , LRG_317t1:c.*968A>G NP_002992.1:n.*968A>G
NR_103459.1:n.1535A>G
NM_001035511.2:c.*861A>G NP_001030588.1:n.*861A>G
NM_001035512.2:c.*968A>G NP_001030589.1:n.*968A>G
NM_001035513.2:c.*968A>G NP_001030590.1:n.*968A>G
NM_001278172.2:c.*861A>G NP_001265101.1:n.*861A>G
NR_103459.2:n.1530A>G
Search 100 bp 5'
Search 100 bp 3'