Canonical Allele Identifier: CA221735680

Gene: NDUFS3

Linked Data

• dbSNP Id: rs1043998765
• gnomAD v3: 11-47582630-T-G
• gnomAD v4: 11-47582630-T-G
• MyVariant Identifiers: chr11:g.47604182T>G (hg19) ; chr11:g.47582630T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582630T>G , CM000673.2:g.47582630T>G	GRCh38
NC_000011.9:g.47604182T>G , CM000673.1:g.47604182T>G	GRCh37
NC_000011.8:g.47560758T>G	NCBI36
NG_011946.1:g.8621T>G
NG_011946.2:g.8621T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.627+162T>G MANE Select	ENSP00000263774.4:n.627+162T>G
ENST00000531351.2:n.1822+162T>G
ENST00000677462.1:n.3101+162T>G
ENST00000678975.1:n.2884+162T>G
ENST00000263774.8:c.627+162T>G	ENSP00000263774.4:n.627+162T>G
ENST00000525212.1:n.282+162T>G
ENST00000525378.5:n.565+162T>G
ENST00000527178.1:n.227+162T>G
ENST00000533507.5:n.1521+162T>G
NM_004551.2:c.627+162T>G	NP_004542.1:n.627+162T>G
NM_004551.3:c.627+162T>G MANE Select	NP_004542.1:n.627+162T>G