Canonical Allele Identifier: CA228555691

Gene: SDHD

Linked Data

• ClinVar Variation Id: 2934143
• ClinVar RCV Id: RCV003795893
• dbSNP Id: rs755584530
• gnomAD v4: 11-112094888-C-G
• MyVariant Identifiers: chr11:g.111965612C>G (hg19) ; chr11:g.112094888C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094888C>G , CM000673.2:g.112094888C>G	GRCh38
NC_000011.9:g.111965612C>G , CM000673.1:g.111965612C>G	GRCh37
NC_000011.8:g.111470822C>G	NCBI36
NG_012337.2:g.13042C>G
NG_012337.3:g.13042C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*137C>G	ENSP00000432946.2:n.*137C>G
ENST00000534010.2:c.314+5877C>G	ENSP00000433202.2:n.314+5877C>G
ENST00000375549.8:c.398C>G MANE Select	ENSP00000364699.3:p.Ala133Gly
ENST00000528021.6:c.314+5877C>G	ENSP00000432465.1:n.314+5877C>G
ENST00000375549.7:c.398C>G	ENSP00000364699.3:p.Ala133Gly
ENST00000525291.5:c.281C>G	ENSP00000436669.1:p.Ala94Gly
ENST00000525987.5:n.319+5877C>G
ENST00000526592.5:c.*96C>G	ENSP00000432005.1:n.*96C>G
ENST00000528021.5:c.314+5877C>G	ENSP00000432465.1:n.314+5877C>G
ENST00000528048.5:c.253C>G	ENSP00000436217.1:p.Leu85Val
ENST00000528182.5:c.391C>G	ENSP00000435475.1:p.Leu131Val
ENST00000530923.5:c.442C>G
ENST00000531744.5:c.314+5877C>G	ENSP00000456957.1:n.314+5877C>G
ENST00000532699.1:c.314+5877C>G	ENSP00000456434.1:n.314+5877C>G
ENST00000534010.1:c.145+5877C>G
NM_001276503.1:c.253C>G	NP_001263432.1:p.Leu85Val
NM_001276504.1:c.281C>G	NP_001263433.1:p.Ala94Gly
NM_001276506.1:c.*96C>G	NP_001263435.1:n.*96C>G
NM_003002.3:c.398C>G	NP_002993.1:p.Ala133Gly
NR_077060.1:n.536C>G
NM_003002.4:c.398C>G MANE Select	NP_002993.1:p.Ala133Gly
NM_001276503.2:c.253C>G	NP_001263432.1:p.Leu85Val
NM_001276504.2:c.281C>G	NP_001263433.1:p.Ala94Gly
NM_001276506.2:c.*96C>G	NP_001263435.1:n.*96C>G
NR_077060.2:n.487C>G