Canonical Allele Identifier: CA2587725832
Gene: NDUFA11 HGNC NCBI

Linked Data

gnomAD v4: 19-5903932-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903932G>C , CM000681.2:g.5903932G>C GRCh38
NC_000019.9:g.5903943G>C , CM000681.1:g.5903943G>C GRCh37
NC_000019.8:g.5854943G>C NCBI36
NG_027808.1:g.5082C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000591160.1:n.75C>G
NM_001193375.1:c.-224C>G NP_001180304.1:n.-224C>G
NM_175614.4:c.-224C>G NP_783313.1:n.-224C>G
NR_034166.2:n.82C>G
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