Canonical Allele Identifier: CA2587725814
Gene: NDUFA11 HGNC NCBI

Linked Data

gnomAD v4: 19-5903919-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903919C>T , CM000681.2:g.5903919C>T GRCh38
NC_000019.9:g.5903930C>T , CM000681.1:g.5903930C>T GRCh37
NC_000019.8:g.5854930C>T NCBI36
NG_027808.1:g.5095G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000591160.1:n.88G>A
NM_001193375.1:c.-211G>A NP_001180304.1:n.-211G>A
NM_175614.4:c.-211G>A NP_783313.1:n.-211G>A
NR_034166.2:n.95G>A
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