Canonical Allele Identifier: CA380362035

Gene: NDUFS3

Linked Data

• MyVariant Identifiers: chr11:g.47604001C>A (hg19) ; chr11:g.47582449C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582449C>A , CM000673.2:g.47582449C>A	GRCh38
NC_000011.9:g.47604001C>A , CM000673.1:g.47604001C>A	GRCh37
NC_000011.8:g.47560577C>A	NCBI36
NG_011946.1:g.8440C>A
NG_011946.2:g.8440C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263774.9:c.608C>A MANE Select	ENSP00000263774.4:p.Pro203His
ENST00000531351.2:n.1803C>A
ENST00000677462.1:n.3082C>A
ENST00000678975.1:n.2865C>A
ENST00000263774.8:c.608C>A	ENSP00000263774.4:p.Pro203His
ENST00000524568.1:n.711C>A
ENST00000525212.1:n.263C>A
ENST00000525378.5:n.546C>A
ENST00000527178.1:n.208C>A
ENST00000533507.5:n.1502C>A
NM_004551.2:c.608C>A	NP_004542.1:p.Pro203His
NM_004551.3:c.608C>A MANE Select	NP_004542.1:p.Pro203His