Canonical Allele Identifier: CA2320171562
Gene: NDUFA11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903921T= , CM000681.2:g.5903921T= GRCh38
NC_000019.9:g.5903932T= , CM000681.1:g.5903932T= GRCh37
NC_000019.8:g.5854932T= NCBI36
NG_027808.1:g.5093A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000591160.1:n.86A=
NM_001193375.1:c.-213A= NP_001180304.1:n.-213A=
NM_175614.4:c.-213A= NP_783313.1:n.-213A=
NR_034166.2:n.93A=