Canonical Allele Identifier: CA221735674

Gene: NDUFS3

Linked Data

• dbSNP Id: rs1046939306
• gnomAD v3: 11-47582569-G-T
• gnomAD v4: 11-47582569-G-T
• MyVariant Identifiers: chr11:g.47604121G>T (hg19) ; chr11:g.47582569G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582569G>T , CM000673.2:g.47582569G>T	GRCh38
NC_000011.9:g.47604121G>T , CM000673.1:g.47604121G>T	GRCh37
NC_000011.8:g.47560697G>T	NCBI36
NG_011946.1:g.8560G>T
NG_011946.2:g.8560G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.627+101G>T MANE Select	ENSP00000263774.4:n.627+101G>T
ENST00000531351.2:n.1822+101G>T
ENST00000677462.1:n.3101+101G>T
ENST00000678975.1:n.2884+101G>T
ENST00000263774.8:c.627+101G>T	ENSP00000263774.4:n.627+101G>T
ENST00000525212.1:n.282+101G>T
ENST00000525378.5:n.565+101G>T
ENST00000527178.1:n.227+101G>T
ENST00000533507.5:n.1521+101G>T
NM_004551.2:c.627+101G>T	NP_004542.1:n.627+101G>T
NM_004551.3:c.627+101G>T MANE Select	NP_004542.1:n.627+101G>T