Canonical Allele Identifier: CA016702
Gene: SDHD HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6897
dbSNP Id: rs80338845

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112088971G>T , CM000673.2:g.112088971G>T GRCh38
NC_000011.9:g.111959695G>T , CM000673.1:g.111959695G>T GRCh37
NC_000011.8:g.111464905G>T NCBI36
NG_012337.2:g.7125G>T
NG_033145.1:g.2828C>A
NG_012337.3:g.7125G>T

Transcript Alleles

HGVS Amino-acid change
NM_001276503.1:c.169+998G>T VV NP_001263432.1:p.=
NM_001276504.1:c.157G>T VV NP_001263433.1:p.Asp53Tyr
NM_001276506.1:c.274G>T VV NP_001263435.1:p.Asp92Tyr
NM_003002.3:c.274G>T VV NP_002993.1:p.Asp92Tyr
NR_077060.1:n.358G>T
NM_003002.4:c.274G>T VV MANE Preferred
ENST00000375549.7:c.274G>T ENSP00000364699.3:p.Asp92Tyr
ENST00000525291.5:c.157G>T ENSP00000436669.1:p.Asp53Tyr
ENST00000525987.5:n.279G>T
ENST00000526592.5:c.274G>T ENSP00000432005.1:p.Asp92Tyr
ENST00000528021.5:c.274G>T ENSP00000432465.1:p.Asp92Tyr
ENST00000528048.5:c.169+998G>T ENSP00000436217.1:p.=
ENST00000528182.5:c.274G>T ENSP00000435475.1:p.Asp92Tyr
ENST00000530923.5:n.264G>T
ENST00000531744.5:c.274G>T ENSP00000456957.1:p.Asp92Tyr
ENST00000532699.1:c.274G>T ENSP00000456434.1:p.Asp92Tyr
ENST00000534010.1:n.105G>T
ENST00000614349.4:c.274G>T ENSP00000480666.1:p.Asp92Tyr