Canonical Allele Identifier: CA3264106
Gene: NDUFS4 HGNC NCBI

Linked Data

dbSNP Id: rs750450668
ExAC: 5:52856456 G / A
gnomAD v2: 5-52856456-G-A
gnomAD v4: 5-53560626-G-A
MyVariant Identifiers: chr5:g.52856456G>A (hg19) chr5:g.53560626G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53560626G>A , CM000667.2:g.53560626G>A GRCh38
NC_000005.9:g.52856456G>A , CM000667.1:g.52856456G>A GRCh37
NC_000005.8:g.52892213G>A NCBI36
NG_008200.1:g.4992G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011543414.1:c.-37G>A XP_011541716.1:n.-37G>A
XM_017009491.1:c.-37G>A XP_016864980.1:n.-37G>A
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