Canonical Allele Identifier: CA1969462266
Gene: NDUFS3 HGNC NCBI

Linked Data

dbSNP Id: rs2097269302

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582632C>T , CM000673.2:g.47582632C>T GRCh38
NC_000011.9:g.47604184C>T , CM000673.1:g.47604184C>T GRCh37
NC_000011.8:g.47560760C>T NCBI36
NG_011946.1:g.8623C>T
NG_011946.2:g.8623C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.627+164C>T MANE Select ENSP00000263774.4:n.627+164C>T
ENST00000531351.2:n.1822+164C>T
ENST00000677462.1:n.3101+164C>T
ENST00000678975.1:n.2884+164C>T
ENST00000263774.8:c.627+164C>T ENSP00000263774.4:n.627+164C>T
ENST00000525212.1:n.282+164C>T
ENST00000525378.5:n.565+164C>T
ENST00000527178.1:n.227+164C>T
ENST00000533507.5:n.1521+164C>T
NM_004551.2:c.627+164C>T NP_004542.1:n.627+164C>T
NM_004551.3:c.627+164C>T MANE Select NP_004542.1:n.627+164C>T