Canonical Allele Identifier: CA380361562

Gene: NDUFS3

Linked Data

• MyVariant Identifiers: chr11:g.47603906G>C (hg19) ; chr11:g.47582354G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582354G>C , CM000673.2:g.47582354G>C	GRCh38
NC_000011.9:g.47603906G>C , CM000673.1:g.47603906G>C	GRCh37
NC_000011.8:g.47560482G>C	NCBI36
NG_011946.1:g.8345G>C
NG_011946.2:g.8345G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263774.9:c.513G>C MANE Select	ENSP00000263774.4:p.Trp171Cys
ENST00000531351.2:n.1708G>C
ENST00000677462.1:n.2987G>C
ENST00000678975.1:n.2770G>C
ENST00000263774.8:c.513G>C	ENSP00000263774.4:p.Trp171Cys
ENST00000524568.1:n.616G>C
ENST00000525212.1:n.168G>C
ENST00000525378.5:n.451G>C
ENST00000527178.1:n.113G>C
ENST00000533507.5:n.1407G>C
NM_004551.2:c.513G>C	NP_004542.1:p.Trp171Cys
NM_004551.3:c.513G>C MANE Select	NP_004542.1:p.Trp171Cys