Canonical Allele Identifier: CA350268543
Gene: NDUFB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.201943669T>A (hg19) chr2:g.201078946T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201078946T>A , CM000664.2:g.201078946T>A GRCh38
NC_000002.11:g.201943669T>A , CM000664.1:g.201943669T>A GRCh37
NC_000002.10:g.201651914T>A NCBI36
NG_032156.1:g.12208T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450023.6:c.64T>A ENSP00000401834.2:p.Trp22Arg
ENST00000682325.1:c.64T>A ENSP00000507925.1:p.Trp22Arg
ENST00000684175.1:c.64T>A ENSP00000508132.1:p.Trp22Arg
ENST00000684420.1:c.64T>A ENSP00000508208.1:p.Trp22Arg
ENST00000237889.9:c.64T>A MANE Select ENSP00000237889.4:p.Trp22Arg
ENST00000237889.8:c.64T>A ENSP00000237889.4:p.Trp22Arg
ENST00000433898.5:c.64T>A ENSP00000410600.1:p.Trp22Arg
ENST00000450023.5:c.64T>A ENSP00000401834.1:p.Trp22Arg
ENST00000454214.1:c.64T>A ENSP00000407336.1:p.Trp22Arg
NM_001257102.1:c.64T>A NP_001244031.1:p.Trp22Arg
NM_002491.2:c.64T>A NP_002482.1:p.Trp22Arg
XM_011511230.1:c.64T>A XP_011509532.1:p.Trp22Arg
XM_011511230.3:c.64T>A XP_011509532.1:p.Trp22Arg
XM_017004186.2:c.64T>A XP_016859675.1:p.Trp22Arg
NM_002491.3:c.64T>A MANE Select NP_002482.1:p.Trp22Arg
NM_001257102.2:c.64T>A NP_001244031.1:p.Trp22Arg
Search 100 bp 5'
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