Canonical Allele Identifier: CA2587725800
Gene: NDUFA11 HGNC NCBI

Linked Data

gnomAD v4: 19-5903912-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903912A>T , CM000681.2:g.5903912A>T GRCh38
NC_000019.9:g.5903923A>T , CM000681.1:g.5903923A>T GRCh37
NC_000019.8:g.5854923A>T NCBI36
NG_027808.1:g.5102T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000591160.1:n.95T>A
NM_001193375.1:c.-204T>A NP_001180304.1:n.-204T>A
NM_175614.4:c.-204T>A NP_783313.1:n.-204T>A
NR_034166.2:n.102T>A