Canonical Allele Identifier: CA599375153

Gene: NDUFS3

Linked Data

• dbSNP Id: rs1410456290
• gnomAD v2: 11-47603600-A-C
• gnomAD v4: 11-47582048-A-C
• MyVariant Identifiers: chr11:g.47603600A>C (hg19) ; chr11:g.47582048A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582048A>C , CM000673.2:g.47582048A>C	GRCh38
NC_000011.9:g.47603600A>C , CM000673.1:g.47603600A>C	GRCh37
NC_000011.8:g.47560176A>C	NCBI36
NG_011946.1:g.8039A>C
NG_011946.2:g.8039A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263774.9:c.382-40A>C MANE Select	ENSP00000263774.4:n.382-40A>C
ENST00000531351.2:n.1402A>C
ENST00000677462.1:n.2816A>C
ENST00000678975.1:n.2599A>C
ENST00000263774.8:c.382-40A>C	ENSP00000263774.4:n.382-40A>C
ENST00000524568.1:n.485-40A>C
ENST00000525378.5:n.280A>C
ENST00000533507.5:n.1276-40A>C
NM_004551.2:c.382-40A>C	NP_004542.1:n.382-40A>C
NM_004551.3:c.382-40A>C MANE Select	NP_004542.1:n.382-40A>C