Canonical Allele Identifier: CA1969462259
Gene: NDUFS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582624G= , CM000673.2:g.47582624G= GRCh38
NC_000011.9:g.47604176G= , CM000673.1:g.47604176G= GRCh37
NC_000011.8:g.47560752G= NCBI36
NG_011946.1:g.8615G=
NG_011946.2:g.8615G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.627+156G= MANE Select ENSP00000263774.4:n.627+156G=
ENST00000531351.2:n.1822+156G=
ENST00000677462.1:n.3101+156G=
ENST00000678975.1:n.2884+156G=
ENST00000263774.8:c.627+156G= ENSP00000263774.4:n.627+156G=
ENST00000525212.1:n.282+156G=
ENST00000525378.5:n.565+156G=
ENST00000527178.1:n.227+156G=
ENST00000533507.5:n.1521+156G=
NM_004551.2:c.627+156G= NP_004542.1:n.627+156G=
NM_004551.3:c.627+156G= MANE Select NP_004542.1:n.627+156G=