Canonical Allele Identifier: CA2613426939

Gene: NDUFS3

Linked Data

• gnomAD v4: 11-47582592-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582592T>C , CM000673.2:g.47582592T>C	GRCh38
NC_000011.9:g.47604144T>C , CM000673.1:g.47604144T>C	GRCh37
NC_000011.8:g.47560720T>C	NCBI36
NG_011946.1:g.8583T>C
NG_011946.2:g.8583T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.627+124T>C MANE Select	ENSP00000263774.4:n.627+124T>C
ENST00000531351.2:n.1822+124T>C
ENST00000677462.1:n.3101+124T>C
ENST00000678975.1:n.2884+124T>C
ENST00000263774.8:c.627+124T>C	ENSP00000263774.4:n.627+124T>C
ENST00000525212.1:n.282+124T>C
ENST00000525378.5:n.565+124T>C
ENST00000527178.1:n.227+124T>C
ENST00000533507.5:n.1521+124T>C
NM_004551.2:c.627+124T>C	NP_004542.1:n.627+124T>C
NM_004551.3:c.627+124T>C MANE Select	NP_004542.1:n.627+124T>C