Canonical Allele Identifier: CA812047309
Gene: NDUFS4 HGNC NCBI

Linked Data

dbSNP Id: rs1299095609
gnomAD v3: 5-53560616-C-A
gnomAD v4: 5-53560616-C-A
MyVariant Identifiers: chr5:g.52856446C>A (hg19) chr5:g.53560616C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53560616C>A , CM000667.2:g.53560616C>A GRCh38
NC_000005.9:g.52856446C>A , CM000667.1:g.52856446C>A GRCh37
NC_000005.8:g.52892203C>A NCBI36
NG_008200.1:g.4982C>A

Transcript Alleles

HGVS Amino-acid Change
XM_017009491.1:c.-47C>A XP_016864980.1:n.-47C>A
Search 100 bp 5'
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