Canonical Allele Identifier: CA1980452604

Gene: NDUFS8

Linked Data

• dbSNP Id: rs1590792257
• gnomAD v4: 11-68036618-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036618C>A , CM000673.2:g.68036618C>A	GRCh38
NC_000011.9:g.67804085C>A , CM000673.1:g.67804085C>A	GRCh37
NC_000011.8:g.67560661C>A	NCBI36
NG_007878.1:g.2603C>A , LRG_115:g.2603C>A
NG_017040.1:g.11002C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.*25C>A MANE Select	ENSP00000315774.5:n.*25C>A
ENST00000313468.9:c.*25C>A	ENSP00000315774.5:n.*25C>A
ENST00000524810.5:c.590C>A
ENST00000528492.1:c.*25C>A	ENSP00000432848.1:n.*25C>A
ENST00000531282.1:n.510C>A
NM_002496.3:c.*25C>A	NP_002487.1:n.*25C>A
XM_005274013.1:c.*25C>A	XP_005274070.1:n.*25C>A
XM_005274014.1:c.*25C>A	XP_005274071.1:n.*25C>A
XM_005274015.1:c.*25C>A	XP_005274072.1:n.*25C>A
XM_011545053.1:c.*25C>A	XP_011543355.1:n.*25C>A
NM_002496.4:c.*25C>A MANE Select	NP_002487.1:n.*25C>A