Canonical Allele Identifier: CA3264110
Gene: NDUFS4 HGNC NCBI

Linked Data

dbSNP Id: rs181175346
ExAC: 5:52856461 G / T
gnomAD v2: 5-52856461-G-T
gnomAD v3: 5-53560631-G-T
gnomAD v4: 5-53560631-G-T
MyVariant Identifiers: chr5:g.52856461G>T (hg19) chr5:g.53560631G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53560631G>T , CM000667.2:g.53560631G>T GRCh38
NC_000005.9:g.52856461G>T , CM000667.1:g.52856461G>T GRCh37
NC_000005.8:g.52892218G>T NCBI36
NG_008200.1:g.4997G>T

Transcript Alleles

HGVS Amino-acid Change
XM_005248525.3:c.-32G>T XP_005248582.1:n.-32G>T
XM_011543414.1:c.-32G>T XP_011541716.1:n.-32G>T
XM_017009491.1:c.-32G>T XP_016864980.1:n.-32G>T
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