Canonical Allele Identifier: CA2587725805
Gene: NDUFA11 HGNC NCBI

Linked Data

gnomAD v4: 19-5903915-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903915A>G , CM000681.2:g.5903915A>G GRCh38
NC_000019.9:g.5903926A>G , CM000681.1:g.5903926A>G GRCh37
NC_000019.8:g.5854926A>G NCBI36
NG_027808.1:g.5099T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000591160.1:n.92T>C
NM_001193375.1:c.-207T>C NP_001180304.1:n.-207T>C
NM_175614.4:c.-207T>C NP_783313.1:n.-207T>C
NR_034166.2:n.99T>C
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