Canonical Allele Identifier: CA380361555

Gene: NDUFS3

Linked Data

• gnomAD v4: 11-47582353-G-C
• MyVariant Identifiers: chr11:g.47603905G>C (hg19) ; chr11:g.47582353G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582353G>C , CM000673.2:g.47582353G>C	GRCh38
NC_000011.9:g.47603905G>C , CM000673.1:g.47603905G>C	GRCh37
NC_000011.8:g.47560481G>C	NCBI36
NG_011946.1:g.8344G>C
NG_011946.2:g.8344G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263774.9:c.512G>C MANE Select	ENSP00000263774.4:p.Trp171Ser
ENST00000531351.2:n.1707G>C
ENST00000677462.1:n.2986G>C
ENST00000678975.1:n.2769G>C
ENST00000263774.8:c.512G>C	ENSP00000263774.4:p.Trp171Ser
ENST00000524568.1:n.615G>C
ENST00000525212.1:n.167G>C
ENST00000525378.5:n.450G>C
ENST00000527178.1:n.112G>C
ENST00000533507.5:n.1406G>C
NM_004551.2:c.512G>C	NP_004542.1:p.Trp171Ser
NM_004551.3:c.512G>C MANE Select	NP_004542.1:p.Trp171Ser