Canonical Allele Identifier: CA13484027

Gene: NDUFS3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47583875G>A , CM000673.2:g.47583875G>A	GRCh38
NC_000011.9:g.47605427G>A , CM000673.1:g.47605427G>A	GRCh37
NC_000011.8:g.47562003G>A	NCBI36
NG_011946.1:g.9866G>A
NG_011946.2:g.9866G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.628-439G>A MANE Select	ENSP00000263774.4:n.628-439G>A
ENST00000531351.2:n.1823-439G>A
ENST00000677462.1:n.3102-439G>A
ENST00000678975.1:n.2885-439G>A
ENST00000263774.8:c.628-439G>A	ENSP00000263774.4:n.628-439G>A
ENST00000525212.1:n.283-439G>A
ENST00000525378.5:n.566-439G>A
ENST00000527178.1:n.228-439G>A
ENST00000533507.5:n.1522-439G>A
NM_004551.2:c.628-439G>A	NP_004542.1:n.628-439G>A
NM_004551.3:c.628-439G>A MANE Select	NP_004542.1:n.628-439G>A