Canonical Allele Identifier: CA1969462227
Gene: NDUFS3 HGNC NCBI

Linked Data

dbSNP Id: rs2097269257

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582535G>A , CM000673.2:g.47582535G>A GRCh38
NC_000011.9:g.47604087G>A , CM000673.1:g.47604087G>A GRCh37
NC_000011.8:g.47560663G>A NCBI36
NG_011946.1:g.8526G>A
NG_011946.2:g.8526G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.627+67G>A MANE Select ENSP00000263774.4:n.627+67G>A
ENST00000531351.2:n.1822+67G>A
ENST00000677462.1:n.3101+67G>A
ENST00000678975.1:n.2884+67G>A
ENST00000263774.8:c.627+67G>A ENSP00000263774.4:n.627+67G>A
ENST00000525212.1:n.282+67G>A
ENST00000525378.5:n.565+67G>A
ENST00000527178.1:n.227+67G>A
ENST00000533507.5:n.1521+67G>A
NM_004551.2:c.627+67G>A NP_004542.1:n.627+67G>A
NM_004551.3:c.627+67G>A MANE Select NP_004542.1:n.627+67G>A