Canonical Allele Identifier: CA2724176159
Gene: NDUFS3 HGNC NCBI

Linked Data

dbSNP Id: rs2153795409

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582508A>G , CM000673.2:g.47582508A>G GRCh38
NC_000011.9:g.47604060A>G , CM000673.1:g.47604060A>G GRCh37
NC_000011.8:g.47560636A>G NCBI36
NG_011946.1:g.8499A>G
NG_011946.2:g.8499A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.627+40A>G MANE Select ENSP00000263774.4:n.627+40A>G
ENST00000531351.2:n.1822+40A>G
ENST00000677462.1:n.3101+40A>G
ENST00000678975.1:n.2884+40A>G
ENST00000263774.8:c.627+40A>G ENSP00000263774.4:n.627+40A>G
ENST00000525212.1:n.282+40A>G
ENST00000525378.5:n.565+40A>G
ENST00000527178.1:n.227+40A>G
ENST00000533507.5:n.1521+40A>G
NM_004551.2:c.627+40A>G NP_004542.1:n.627+40A>G
NM_004551.3:c.627+40A>G MANE Select NP_004542.1:n.627+40A>G