Canonical Allele Identifier: CA2574899203
Gene: NDUFS8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68036624A>G , CM000673.2:g.68036624A>G GRCh38
NC_000011.9:g.67804091A>G , CM000673.1:g.67804091A>G GRCh37
NC_000011.8:g.67560667A>G NCBI36
NG_007878.1:g.2609A>G , LRG_115:g.2609A>G
NG_017040.1:g.11008A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313468.10:c.*31A>G MANE Select ENSP00000315774.5:n.*31A>G
ENST00000313468.9:c.*31A>G ENSP00000315774.5:n.*31A>G
ENST00000524810.5:c.596A>G
ENST00000528492.1:c.*31A>G ENSP00000432848.1:n.*31A>G
ENST00000531282.1:n.516A>G
NM_002496.3:c.*31A>G NP_002487.1:n.*31A>G
XM_005274013.1:c.*31A>G XP_005274070.1:n.*31A>G
XM_005274014.1:c.*31A>G XP_005274071.1:n.*31A>G
XM_005274015.1:c.*31A>G XP_005274072.1:n.*31A>G
XM_011545053.1:c.*31A>G XP_011543355.1:n.*31A>G
NM_002496.4:c.*31A>G MANE Select NP_002487.1:n.*31A>G