Canonical Allele Identifier: CA2320171565
Gene: NDUFA11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903926C= , CM000681.2:g.5903926C= GRCh38
NC_000019.9:g.5903937C= , CM000681.1:g.5903937C= GRCh37
NC_000019.8:g.5854937C= NCBI36
NG_027808.1:g.5088G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000591160.1:n.81G=
NM_001193375.1:c.-218G= NP_001180304.1:n.-218G=
NM_175614.4:c.-218G= NP_783313.1:n.-218G=
NR_034166.2:n.88G=