Canonical Allele Identifier: CA016785
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 6913
ClinVar RCV Id: RCV000007322 RCV000222413 RCV000756632 RCV002512871
dbSNP Id: rs104894308
MyVariant Identifiers: chr11:g.111958657G>A (hg19) chr11:g.112087933G>A (hg38)
PubMed: PMID:12111639 PMID:18211978
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112087933G>A , CM000673.2:g.112087933G>A GRCh38
NC_000011.9:g.111958657G>A , CM000673.1:g.111958657G>A GRCh37
NC_000011.8:g.111463867G>A NCBI36
NG_012337.2:g.6087G>A
NG_033145.1:g.3866C>T
NG_012337.3:g.6087G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.129G>A ENSP00000432946.2:p.Trp43Ter
ENST00000534010.2:c.129G>A ENSP00000433202.2:p.Trp43Ter
ENST00000375549.8:c.129G>A MANE Select ENSP00000364699.3:p.Trp43Ter
ENST00000528021.6:c.129G>A ENSP00000432465.1:p.Trp43Ter
ENST00000640554.1:c.129G>A ENSP00000491141.1:p.Trp43Ter
ENST00000375549.7:c.129G>A ENSP00000364699.3:p.Trp43Ter
ENST00000525291.5:c.53-934G>A ENSP00000436669.1:n.53-934G>A
ENST00000525987.5:n.134G>A
ENST00000526592.5:c.129G>A ENSP00000432005.1:p.Trp43Ter
ENST00000528021.5:c.129G>A ENSP00000432465.1:p.Trp43Ter
ENST00000528048.5:c.129G>A ENSP00000436217.1:p.Trp43Ter
ENST00000528182.5:c.129G>A ENSP00000435475.1:p.Trp43Ter
ENST00000530923.5:c.119G>A
ENST00000531744.5:c.129G>A ENSP00000456957.1:p.Trp43Ter
ENST00000532699.1:c.129G>A ENSP00000456434.1:p.Trp43Ter
ENST00000614349.4:c.129G>A ENSP00000480666.1:p.Trp43Ter
NM_001276503.1:c.129G>A NP_001263432.1:p.Trp43Ter
NM_001276504.1:c.53-934G>A NP_001263433.1:n.53-934G>A
NM_001276506.1:c.129G>A NP_001263435.1:p.Trp43Ter
NM_003002.3:c.129G>A NP_002993.1:p.Trp43Ter
NR_077060.1:n.213G>A
NM_003002.4:c.129G>A MANE Select NP_002993.1:p.Trp43Ter
NM_001276503.2:c.129G>A NP_001263432.1:p.Trp43Ter
NM_001276504.2:c.53-934G>A NP_001263433.1:n.53-934G>A
NM_001276506.2:c.129G>A NP_001263435.1:p.Trp43Ter
NR_077060.2:n.164G>A
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