Canonical Allele Identifier: CA2587725838
Gene: NDUFA11 HGNC NCBI

Linked Data

gnomAD v4: 19-5903935-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903935G>A , CM000681.2:g.5903935G>A GRCh38
NC_000019.9:g.5903946G>A , CM000681.1:g.5903946G>A GRCh37
NC_000019.8:g.5854946G>A NCBI36
NG_027808.1:g.5079C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000591160.1:n.72C>T
NM_001193375.1:c.-227C>T NP_001180304.1:n.-227C>T
NM_175614.4:c.-227C>T NP_783313.1:n.-227C>T
NR_034166.2:n.79C>T