Canonical Allele Identifier: CA2580081082

Gene: NDUFB8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100527094T>G , CM000672.2:g.100527094T>G	GRCh38
NC_000010.10:g.102286851T>G , CM000672.1:g.102286851T>G	GRCh37
NC_000010.9:g.102276841T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299166.9:c.213-20A>C MANE Select	ENSP00000299166.4:n.213-20A>C
ENST00000299166.8:c.213-20A>C	ENSP00000299166.4:n.213-20A>C
ENST00000370320.4:c.213-20A>C	ENSP00000359344.4:n.213-20A>C
ENST00000370322.5:c.120-20A>C	ENSP00000359346.1:n.120-20A>C
ENST00000466088.5:n.224-20A>C
ENST00000527595.5:c.213-20A>C	ENSP00000455090.1:n.213-20A>C
ENST00000528174.5:c.*11-20A>C	ENSP00000456355.1:n.*11-20A>C
ENST00000528425.5:c.*11-20A>C	ENSP00000434072.1:n.*11-20A>C
ENST00000529437.1:n.245-20A>C
ENST00000529568.5:c.213-20A>C	ENSP00000455597.1:n.213-20A>C
ENST00000531418.5:n.255-20A>C
ENST00000533549.1:c.*11-20A>C	ENSP00000456407.1:n.*11-20A>C
ENST00000557395.5:c.213-20A>C	ENSP00000456832.1:n.213-20A>C
NM_001284367.1:c.213-20A>C	NP_001271296.1:n.213-20A>C
NM_001284368.1:c.120-20A>C	NP_001271297.1:n.120-20A>C
NM_005004.3:c.213-20A>C	NP_004995.1:n.213-20A>C
NM_005004.4:c.213-20A>C MANE Select	NP_004995.1:n.213-20A>C
NM_001284367.2:c.213-20A>C	NP_001271296.1:n.213-20A>C