Canonical Allele Identifier: CA1969462138

Gene: NDUFS3

Linked Data

• dbSNP Id: rs1006695051
• gnomAD v4: 11-47582311-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582311C>T , CM000673.2:g.47582311C>T	GRCh38
NC_000011.9:g.47603863C>T , CM000673.1:g.47603863C>T	GRCh37
NC_000011.8:g.47560439C>T	NCBI36
NG_011946.1:g.8302C>T
NG_011946.2:g.8302C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.508-38C>T MANE Select	ENSP00000263774.4:n.508-38C>T
ENST00000531351.2:n.1665C>T
ENST00000677462.1:n.2982-38C>T
ENST00000678975.1:n.2765-38C>T
ENST00000263774.8:c.508-38C>T	ENSP00000263774.4:n.508-38C>T
ENST00000524568.1:n.611-38C>T
ENST00000525212.1:n.163-38C>T
ENST00000525378.5:n.446-38C>T
ENST00000527178.1:n.70C>T
ENST00000533507.5:n.1402-38C>T
NM_004551.2:c.508-38C>T	NP_004542.1:n.508-38C>T
NM_004551.3:c.508-38C>T MANE Select	NP_004542.1:n.508-38C>T