Canonical Allele Identifier: CA016709
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 180590
ClinVar RCV Id: RCV000171136 RCV000186596
dbSNP Id: rs786205436
MyVariant Identifiers: chr11:g.111959696A>G (hg19) chr11:g.112088972A>G (hg38)
PubMed: PMID:26008905
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112088972A>G , CM000673.2:g.112088972A>G GRCh38
NC_000011.9:g.111959696A>G , CM000673.1:g.111959696A>G GRCh37
NC_000011.8:g.111464906A>G NCBI36
NG_012337.2:g.7126A>G
NG_033145.1:g.2827T>C
NG_012337.3:g.7126A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.275A>G ENSP00000432946.2:p.Asp92Gly
ENST00000534010.2:c.275A>G ENSP00000433202.2:p.Asp92Gly
ENST00000375549.8:c.275A>G MANE Select ENSP00000364699.3:p.Asp92Gly
ENST00000528021.6:c.275A>G ENSP00000432465.1:p.Asp92Gly
ENST00000640554.1:c.*347A>G ENSP00000491141.1:n.*347A>G
ENST00000375549.7:c.275A>G ENSP00000364699.3:p.Asp92Gly
ENST00000525291.5:c.158A>G ENSP00000436669.1:p.Asp53Gly
ENST00000525987.5:n.280A>G
ENST00000526592.5:c.275A>G ENSP00000432005.1:p.Asp92Gly
ENST00000528021.5:c.275A>G ENSP00000432465.1:p.Asp92Gly
ENST00000528048.5:c.169+999A>G ENSP00000436217.1:n.169+999A>G
ENST00000528182.5:c.275A>G ENSP00000435475.1:p.Asp92Gly
ENST00000530923.5:c.265A>G
ENST00000531744.5:c.275A>G ENSP00000456957.1:p.Asp92Gly
ENST00000532699.1:c.275A>G ENSP00000456434.1:p.Asp92Gly
ENST00000534010.1:c.106A>G
ENST00000614349.4:c.275A>G ENSP00000480666.1:p.Asp92Gly
NM_001276503.1:c.169+999A>G NP_001263432.1:n.169+999A>G
NM_001276504.1:c.158A>G NP_001263433.1:p.Asp53Gly
NM_001276506.1:c.275A>G NP_001263435.1:p.Asp92Gly
NM_003002.3:c.275A>G NP_002993.1:p.Asp92Gly
NR_077060.1:n.359A>G
NM_003002.4:c.275A>G MANE Select NP_002993.1:p.Asp92Gly
NM_001276503.2:c.169+999A>G NP_001263432.1:n.169+999A>G
NM_001276504.2:c.158A>G NP_001263433.1:p.Asp53Gly
NM_001276506.2:c.275A>G NP_001263435.1:p.Asp92Gly
NR_077060.2:n.310A>G
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