Canonical Allele Identifier: CA382619281
Gene: SDHD HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.111965626G>C (hg19) chr11:g.112094902G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112094902G>C , CM000673.2:g.112094902G>C GRCh38
NC_000011.9:g.111965626G>C , CM000673.1:g.111965626G>C GRCh37
NC_000011.8:g.111470836G>C NCBI36
NG_012337.2:g.13056G>C
NG_012337.3:g.13056G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.*151G>C ENSP00000432946.2:n.*151G>C
ENST00000534010.2:c.314+5891G>C ENSP00000433202.2:n.314+5891G>C
ENST00000375549.8:c.412G>C MANE Select ENSP00000364699.3:p.Gly138Arg
ENST00000528021.6:c.314+5891G>C ENSP00000432465.1:n.314+5891G>C
ENST00000375549.7:c.412G>C ENSP00000364699.3:p.Gly138Arg
ENST00000525291.5:c.295G>C ENSP00000436669.1:p.Gly99Arg
ENST00000525987.5:n.319+5891G>C
ENST00000526592.5:c.*110G>C ENSP00000432005.1:n.*110G>C
ENST00000528021.5:c.314+5891G>C ENSP00000432465.1:n.314+5891G>C
ENST00000528048.5:c.*9G>C ENSP00000436217.1:n.*9G>C
ENST00000528182.5:c.*9G>C ENSP00000435475.1:n.*9G>C
ENST00000530923.5:c.456G>C
ENST00000531744.5:c.314+5891G>C ENSP00000456957.1:n.314+5891G>C
ENST00000532699.1:c.314+5891G>C ENSP00000456434.1:n.314+5891G>C
ENST00000534010.1:c.145+5891G>C
NM_001276503.1:c.*9G>C NP_001263432.1:n.*9G>C
NM_001276504.1:c.295G>C NP_001263433.1:p.Gly99Arg
NM_001276506.1:c.*110G>C NP_001263435.1:n.*110G>C
NM_003002.3:c.412G>C NP_002993.1:p.Gly138Arg
NR_077060.1:n.550G>C
NM_003002.4:c.412G>C MANE Select NP_002993.1:p.Gly138Arg
NM_001276503.2:c.*9G>C NP_001263432.1:n.*9G>C
NM_001276504.2:c.295G>C NP_001263433.1:p.Gly99Arg
NM_001276506.2:c.*110G>C NP_001263435.1:n.*110G>C
NR_077060.2:n.501G>C
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