Canonical Allele Identifier: CA2320171513
Gene: NDUFA11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903860G= , CM000681.2:g.5903860G= GRCh38
NC_000019.9:g.5903871G= , CM000681.1:g.5903871G= GRCh37
NC_000019.8:g.5854871G= NCBI36
NG_027808.1:g.5154C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000591160.1:n.147C=
NM_001193375.1:c.-152C= NP_001180304.1:n.-152C=
NM_175614.4:c.-152C= NP_783313.1:n.-152C=
NR_034166.2:n.154C=