Canonical Allele Identifier: CA2753866836

Gene: NDUFB3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201085654T>A , CM000664.2:g.201085654T>A	GRCh38
NC_000002.11:g.201950377T>A , CM000664.1:g.201950377T>A	GRCh37
NC_000002.10:g.201658622T>A	NCBI36
NG_032156.1:g.18916T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682325.1:c.*39T>A	ENSP00000507925.1:n.*39T>A
ENST00000684175.1:c.*39T>A	ENSP00000508132.1:n.*39T>A
ENST00000684420.1:c.*39T>A	ENSP00000508208.1:n.*39T>A
ENST00000237889.9:c.*39T>A MANE Select	ENSP00000237889.4:n.*39T>A
ENST00000237889.8:c.*39T>A	ENSP00000237889.4:n.*39T>A
ENST00000433898.5:c.*39T>A	ENSP00000410600.1:n.*39T>A
ENST00000454214.1:c.*39T>A	ENSP00000407336.1:n.*39T>A
NM_001257102.1:c.*39T>A	NP_001244031.1:n.*39T>A
NM_002491.2:c.*39T>A	NP_002482.1:n.*39T>A
XM_011511230.1:c.*39T>A	XP_011509532.1:n.*39T>A
XM_011511230.3:c.*39T>A	XP_011509532.1:n.*39T>A
XM_017004186.2:c.*39T>A	XP_016859675.1:n.*39T>A
NM_002491.3:c.*39T>A MANE Select	NP_002482.1:n.*39T>A
NM_001257102.2:c.*39T>A	NP_001244031.1:n.*39T>A