Canonical Allele Identifier: CA475443177

Gene: NDUFS8

Linked Data

• gnomAD v4: 11-68036588-C-A
• MyVariant Identifiers: chr11:g.67804055C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036588C>A , CM000673.2:g.68036588C>A	GRCh38
NC_000011.9:g.67804055C>A , CM000673.1:g.67804055C>A	GRCh37
NC_000011.8:g.67560631C>A	NCBI36
NG_007878.1:g.2573C>A , LRG_115:g.2573C>A
NG_017040.1:g.10972C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.628C>A MANE Select	ENSP00000315774.5:p.Arg210=
ENST00000313468.9:c.628C>A	ENSP00000315774.5:p.Arg210=
ENST00000524810.5:c.560C>A
ENST00000528492.1:c.190C>A	ENSP00000432848.1:p.Arg64=
ENST00000531282.1:n.480C>A
NM_002496.3:c.628C>A	NP_002487.1:p.Arg210=
XM_005274013.1:c.628C>A	XP_005274070.1:p.Arg210=
XM_005274014.1:c.628C>A	XP_005274071.1:p.Arg210=
XM_005274015.1:c.508C>A	XP_005274072.1:p.Arg170=
XM_011545053.1:c.628C>A	XP_011543355.1:p.Arg210=
NM_002496.4:c.628C>A MANE Select	NP_002487.1:p.Arg210=