Canonical Allele Identifier: CA380361517

Gene: NDUFS3

Linked Data

• MyVariant Identifiers: chr11:g.47603899A>C (hg19) ; chr11:g.47582347A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582347A>C , CM000673.2:g.47582347A>C	GRCh38
NC_000011.9:g.47603899A>C , CM000673.1:g.47603899A>C	GRCh37
NC_000011.8:g.47560475A>C	NCBI36
NG_011946.1:g.8338A>C
NG_011946.2:g.8338A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.508-2A>C MANE Select	ENSP00000263774.4:n.508-2A>C
ENST00000531351.2:n.1701A>C
ENST00000677462.1:n.2982-2A>C
ENST00000678975.1:n.2765-2A>C
ENST00000263774.8:c.508-2A>C	ENSP00000263774.4:n.508-2A>C
ENST00000524568.1:n.611-2A>C
ENST00000525212.1:n.163-2A>C
ENST00000525378.5:n.446-2A>C
ENST00000527178.1:n.106A>C
ENST00000533507.5:n.1402-2A>C
NM_004551.2:c.508-2A>C	NP_004542.1:n.508-2A>C
NM_004551.3:c.508-2A>C MANE Select	NP_004542.1:n.508-2A>C