Canonical Allele Identifier: CA2587725754
Gene: NDUFA11 HGNC NCBI

Linked Data

gnomAD v4: 19-5903863-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903863C>A , CM000681.2:g.5903863C>A GRCh38
NC_000019.9:g.5903874C>A , CM000681.1:g.5903874C>A GRCh37
NC_000019.8:g.5854874C>A NCBI36
NG_027808.1:g.5151G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000591160.1:n.144G>T
NM_001193375.1:c.-155G>T NP_001180304.1:n.-155G>T
NM_175614.4:c.-155G>T NP_783313.1:n.-155G>T
NR_034166.2:n.151G>T
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