Canonical Allele Identifier: CA1969462118
Gene: NDUFS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582283A= , CM000673.2:g.47582283A= GRCh38
NC_000011.9:g.47603835A= , CM000673.1:g.47603835A= GRCh37
NC_000011.8:g.47560411A= NCBI36
NG_011946.1:g.8274A=
NG_011946.2:g.8274A=

Transcript Alleles

HGVS Amino-acid change
ENST00000263774.9:c.508-66A= MANE Select ENSP00000263774.4:n.508-66A=
ENST00000531351.2:n.1637A=
ENST00000677462.1:n.2982-66A=
ENST00000678975.1:n.2765-66A=
ENST00000263774.8:c.508-66A= ENSP00000263774.4:n.508-66A=
ENST00000524568.1:n.611-66A=
ENST00000525212.1:n.163-66A=
ENST00000525378.5:n.446-66A=
ENST00000527178.1:n.42A=
ENST00000533507.5:n.1402-66A=
NM_004551.2:c.508-66A= NP_004542.1:n.508-66A=
NM_004551.3:c.508-66A= MANE Select NP_004542.1:n.508-66A=