Canonical Allele Identifier: CA2320171625
Gene: NDUFA11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5904013G= , CM000681.2:g.5904013G= GRCh38
NC_000019.9:g.5904024G= , CM000681.1:g.5904024G= GRCh37
NC_000019.8:g.5855024G= NCBI36
NG_027808.1:g.5001C=

Transcript Alleles

HGVS Amino-acid Change
NM_001193375.1:c.-305C= NP_001180304.1:n.-305C=
NM_175614.4:c.-305C= NP_783313.1:n.-305C=
NR_034166.2:n.1C=