Canonical Allele Identifier: CA2587725806
Gene: NDUFA11 HGNC NCBI

Linked Data

gnomAD v4: 19-5903916-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903916G>T , CM000681.2:g.5903916G>T GRCh38
NC_000019.9:g.5903927G>T , CM000681.1:g.5903927G>T GRCh37
NC_000019.8:g.5854927G>T NCBI36
NG_027808.1:g.5098C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000591160.1:n.91C>A
NM_001193375.1:c.-208C>A NP_001180304.1:n.-208C>A
NM_175614.4:c.-208C>A NP_783313.1:n.-208C>A
NR_034166.2:n.98C>A
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