Canonical Allele Identifier: CA599064828

Gene: NDUFS3

Linked Data

• dbSNP Id: rs1182292824
• gnomAD v2: 11-47604038-G-A
• gnomAD v4: 11-47582486-G-A
• MyVariant Identifiers: chr11:g.47604038G>A (hg19) ; chr11:g.47582486G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582486G>A , CM000673.2:g.47582486G>A	GRCh38
NC_000011.9:g.47604038G>A , CM000673.1:g.47604038G>A	GRCh37
NC_000011.8:g.47560614G>A	NCBI36
NG_011946.1:g.8477G>A
NG_011946.2:g.8477G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.627+18G>A MANE Select	ENSP00000263774.4:n.627+18G>A
ENST00000531351.2:n.1822+18G>A
ENST00000677462.1:n.3101+18G>A
ENST00000678975.1:n.2884+18G>A
ENST00000263774.8:c.627+18G>A	ENSP00000263774.4:n.627+18G>A
ENST00000525212.1:n.282+18G>A
ENST00000525378.5:n.565+18G>A
ENST00000527178.1:n.227+18G>A
ENST00000533507.5:n.1521+18G>A
NM_004551.2:c.627+18G>A	NP_004542.1:n.627+18G>A
NM_004551.3:c.627+18G>A MANE Select	NP_004542.1:n.627+18G>A