Canonical Allele Identifier: CA599375151

Gene: NDUFS3

Linked Data

• dbSNP Id: rs1185790223
• gnomAD v2: 11-47603591-C-T
• gnomAD v4: 11-47582039-C-T
• MyVariant Identifiers: chr11:g.47603591C>T (hg19) ; chr11:g.47582039C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582039C>T , CM000673.2:g.47582039C>T	GRCh38
NC_000011.9:g.47603591C>T , CM000673.1:g.47603591C>T	GRCh37
NC_000011.8:g.47560167C>T	NCBI36
NG_011946.1:g.8030C>T
NG_011946.2:g.8030C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263774.9:c.382-49C>T MANE Select	ENSP00000263774.4:n.382-49C>T
ENST00000531351.2:n.1393C>T
ENST00000677462.1:n.2807C>T
ENST00000678975.1:n.2590C>T
ENST00000263774.8:c.382-49C>T	ENSP00000263774.4:n.382-49C>T
ENST00000524568.1:n.485-49C>T
ENST00000525378.5:n.271C>T
ENST00000533507.5:n.1276-49C>T
NM_004551.2:c.382-49C>T	NP_004542.1:n.382-49C>T
NM_004551.3:c.382-49C>T MANE Select	NP_004542.1:n.382-49C>T