Canonical Allele Identifier: CA2587725852
Gene: NDUFA11 HGNC NCBI

Linked Data

gnomAD v4: 19-5903946-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903946G>T , CM000681.2:g.5903946G>T GRCh38
NC_000019.9:g.5903957G>T , CM000681.1:g.5903957G>T GRCh37
NC_000019.8:g.5854957G>T NCBI36
NG_027808.1:g.5068C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000591160.1:n.61C>A
NM_001193375.1:c.-238C>A NP_001180304.1:n.-238C>A
NM_175614.4:c.-238C>A NP_783313.1:n.-238C>A
NR_034166.2:n.68C>A