Canonical Allele Identifier: CA5020952
Gene: NDUFB6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32570967T>C , CM000671.2:g.32570967T>C GRCh38
NC_000009.11:g.32570965T>C , CM000671.1:g.32570965T>C GRCh37
NC_000009.10:g.32560965T>C NCBI36
NG_011511.1:g.7218A>G

Transcript Alleles

HGVS Amino-acid Change
NM_002493.5:c.266A>G MANE Select NP_002484.1:p.His89Arg
ENST00000379847.8:c.266A>G MANE Select ENSP00000369176.3:p.His89Arg
NM_001199987.1:c.180+1914A>G NP_001186916.1:n.180+1914A>G
NM_001199987.2:c.180+1914A>G NP_001186916.1:n.180+1914A>G
NM_002493.4:c.266A>G NP_002484.1:p.His89Arg
NM_182739.2:c.266A>G NP_877416.1:p.His89Arg
NM_182739.3:c.266A>G NP_877416.1:p.His89Arg
ENST00000350021.2:c.266A>G ENSP00000297983.3:p.His89Arg
ENST00000366466.5:c.180+1914A>G ENSP00000482941.1:n.180+1914A>G
ENST00000379847.7:c.266A>G ENSP00000369176.3:p.His89Arg