Canonical Allele Identifier: CA16613226
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412497
ClinVar RCV Id: RCV000462080 RCV002230838 RCV002323759
dbSNP Id: rs1060503769
MyVariant Identifiers: chr11:g.111965529G>A (hg19) chr11:g.112094805G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112094805G>A , CM000673.2:g.112094805G>A GRCh38
NC_000011.9:g.111965529G>A , CM000673.1:g.111965529G>A GRCh37
NC_000011.8:g.111470739G>A NCBI36
NG_012337.2:g.12959G>A
NG_012337.3:g.12959G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.*54G>A ENSP00000432946.2:n.*54G>A
ENST00000534010.2:c.314+5794G>A ENSP00000433202.2:n.314+5794G>A
ENST00000375549.8:c.315G>A MANE Select ENSP00000364699.3:p.Trp105Ter
ENST00000528021.6:c.314+5794G>A ENSP00000432465.1:n.314+5794G>A
ENST00000375549.7:c.315G>A ENSP00000364699.3:p.Trp105Ter
ENST00000525291.5:c.198G>A ENSP00000436669.1:p.Trp66Ter
ENST00000525987.5:n.319+5794G>A
ENST00000526592.5:c.*13G>A ENSP00000432005.1:n.*13G>A
ENST00000528021.5:c.314+5794G>A ENSP00000432465.1:n.314+5794G>A
ENST00000528048.5:c.170G>A ENSP00000436217.1:p.Trp57Ter
ENST00000528182.5:c.308G>A ENSP00000435475.1:p.Gly103Glu
ENST00000530923.5:c.359G>A
ENST00000531744.5:c.314+5794G>A ENSP00000456957.1:n.314+5794G>A
ENST00000532699.1:c.314+5794G>A ENSP00000456434.1:n.314+5794G>A
ENST00000534010.1:c.145+5794G>A
NM_001276503.1:c.170G>A NP_001263432.1:p.Trp57Ter
NM_001276504.1:c.198G>A NP_001263433.1:p.Trp66Ter
NM_001276506.1:c.*13G>A NP_001263435.1:n.*13G>A
NM_003002.3:c.315G>A NP_002993.1:p.Trp105Ter
NR_077060.1:n.453G>A
NM_003002.4:c.315G>A MANE Select NP_002993.1:p.Trp105Ter
NM_001276503.2:c.170G>A NP_001263432.1:p.Trp57Ter
NM_001276504.2:c.198G>A NP_001263433.1:p.Trp66Ter
NM_001276506.2:c.*13G>A NP_001263435.1:n.*13G>A
NR_077060.2:n.404G>A
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