Canonical Allele Identifier: CA2320171559
Gene: NDUFA11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903918A= , CM000681.2:g.5903918A= GRCh38
NC_000019.9:g.5903929A= , CM000681.1:g.5903929A= GRCh37
NC_000019.8:g.5854929A= NCBI36
NG_027808.1:g.5096T=

Transcript Alleles

HGVS Amino-acid change
ENST00000591160.1:n.89T=
NM_001193375.1:c.-210T= NP_001180304.1:n.-210T=
NM_175614.4:c.-210T= NP_783313.1:n.-210T=
NR_034166.2:n.96T=