Canonical Allele Identifier: CA380362089

Gene: NDUFS3

Linked Data

• MyVariant Identifiers: chr11:g.47604014T>A (hg19) ; chr11:g.47582462T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582462T>A , CM000673.2:g.47582462T>A	GRCh38
NC_000011.9:g.47604014T>A , CM000673.1:g.47604014T>A	GRCh37
NC_000011.8:g.47560590T>A	NCBI36
NG_011946.1:g.8453T>A
NG_011946.2:g.8453T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.621T>A MANE Select	ENSP00000263774.4:p.Tyr207Ter
ENST00000531351.2:n.1816T>A
ENST00000677462.1:n.3095T>A
ENST00000678975.1:n.2878T>A
ENST00000263774.8:c.621T>A	ENSP00000263774.4:p.Tyr207Ter
ENST00000524568.1:n.724T>A
ENST00000525212.1:n.276T>A
ENST00000525378.5:n.559T>A
ENST00000527178.1:n.221T>A
ENST00000533507.5:n.1515T>A
NM_004551.2:c.621T>A	NP_004542.1:p.Tyr207Ter
NM_004551.3:c.621T>A MANE Select	NP_004542.1:p.Tyr207Ter