Canonical Allele Identifier: CA2000559405
Gene: SDHD HGNC NCBI
TIMM8B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086784A= , CM000673.2:g.112086784A= GRCh38
NC_000011.9:g.111957508A= , CM000673.1:g.111957508A= GRCh37
NC_000011.8:g.111462718A= NCBI36
NG_012337.2:g.4938A=
NG_033145.1:g.5015T=
NG_012337.3:g.4938A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375549.7:c.-124A= (SDHD) ENSP00000364699.3:n.-124A=
ENST00000504148.2:c.-61T= (TIMM8B) ENSP00000422122.2:n.-61T=
ENST00000509359.6:c.-61T= (TIMM8B) ENSP00000421964.2:n.-61T=
ENST00000541231.1:c.-16T= (TIMM8B) ENSP00000438455.1:n.-16T=
NM_012459.2:c.-16T= (TIMM8B) NP_036591.2:n.-16T=
NR_028383.1:n.15T= (TIMM8B)
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