Canonical Allele Identifier: CA2320171554
Gene: NDUFA11 HGNC NCBI

Linked Data

dbSNP Id: rs996493424

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903913G>C , CM000681.2:g.5903913G>C GRCh38
NC_000019.9:g.5903924G>C , CM000681.1:g.5903924G>C GRCh37
NC_000019.8:g.5854924G>C NCBI36
NG_027808.1:g.5101C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000591160.1:n.94C>G
NM_001193375.1:c.-205C>G NP_001180304.1:n.-205C>G
NM_175614.4:c.-205C>G NP_783313.1:n.-205C>G
NR_034166.2:n.101C>G