Canonical Allele Identifier: CA2613426948

Gene: NDUFS3

Linked Data

• gnomAD v4: 11-47582600-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582600C>G , CM000673.2:g.47582600C>G	GRCh38
NC_000011.9:g.47604152C>G , CM000673.1:g.47604152C>G	GRCh37
NC_000011.8:g.47560728C>G	NCBI36
NG_011946.1:g.8591C>G
NG_011946.2:g.8591C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.627+132C>G MANE Select	ENSP00000263774.4:n.627+132C>G
ENST00000531351.2:n.1822+132C>G
ENST00000677462.1:n.3101+132C>G
ENST00000678975.1:n.2884+132C>G
ENST00000263774.8:c.627+132C>G	ENSP00000263774.4:n.627+132C>G
ENST00000525212.1:n.282+132C>G
ENST00000525378.5:n.565+132C>G
ENST00000527178.1:n.227+132C>G
ENST00000533507.5:n.1521+132C>G
NM_004551.2:c.627+132C>G	NP_004542.1:n.627+132C>G
NM_004551.3:c.627+132C>G MANE Select	NP_004542.1:n.627+132C>G