Canonical Allele Identifier: CA6146418

Gene: NDUFS8

Linked Data

• dbSNP Id: rs781529686
• ExAC: 11:67800549 C / A
• gnomAD v2: 11-67800549-C-A
• gnomAD v3: 11-68033082-C-A
• gnomAD v4: 11-68033082-C-A
• MyVariant Identifiers: chr11:g.67800549C>A (hg19) ; chr11:g.68033082C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033082C>A , CM000673.2:g.68033082C>A	GRCh38
NC_000011.9:g.67800549C>A , CM000673.1:g.67800549C>A	GRCh37
NC_000011.8:g.67557125C>A	NCBI36
NG_017040.1:g.7466C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.200-29C>A MANE Select	ENSP00000315774.5:n.200-29C>A
ENST00000313468.9:c.200-29C>A	ENSP00000315774.5:n.200-29C>A
ENST00000432321.6:n.317-29C>A
ENST00000453471.6:c.200-29C>A	ENSP00000403972.2:n.200-29C>A
ENST00000525419.5:c.146-29C>A	ENSP00000433521.1:n.146-29C>A
ENST00000525628.1:c.200-29C>A	ENSP00000432968.1:n.200-29C>A
ENST00000526339.5:c.200-29C>A	ENSP00000436287.1:n.200-29C>A
ENST00000526446.5:c.*255-29C>A	ENSP00000433645.1:n.*255-29C>A
ENST00000528492.1:c.-67+2349C>A	ENSP00000432848.1:n.-67+2349C>A
ENST00000529645.1:c.378-29C>A	ENSP00000431293.1:n.378-29C>A
ENST00000531228.1:c.*42-29C>A	ENSP00000433054.1:n.*42-29C>A
ENST00000532399.1:n.876C>A
NM_002496.3:c.200-29C>A	NP_002487.1:n.200-29C>A
XM_005274013.1:c.200-29C>A	XP_005274070.1:n.200-29C>A
XM_005274014.1:c.200-29C>A	XP_005274071.1:n.200-29C>A
XM_005274015.1:c.80-29C>A	XP_005274072.1:n.80-29C>A
XM_011545053.1:c.200-29C>A	XP_011543355.1:n.200-29C>A
NM_002496.4:c.200-29C>A MANE Select	NP_002487.1:n.200-29C>A