Canonical Allele Identifier: CA6146600
Gene: NDUFS8 HGNC NCBI

Linked Data

dbSNP Id: rs765424108
ExAC: 11:67804112 C / T
gnomAD v2: 11-67804112-C-T
gnomAD v3: 11-68036645-C-T
gnomAD v4: 11-68036645-C-T
MyVariant Identifiers: chr11:g.67804112C>T (hg19) chr11:g.68036645C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68036645C>T , CM000673.2:g.68036645C>T GRCh38
NC_000011.9:g.67804112C>T , CM000673.1:g.67804112C>T GRCh37
NC_000011.8:g.67560688C>T NCBI36
NG_007878.1:g.2630C>T , LRG_115:g.2630C>T
NG_017040.1:g.11029C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002496.3:c.*52C>T NP_002487.1:n.*52C>T
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