Canonical Allele Identifier: CA10649164
Gene: NDUFA11 HGNC NCBI

Linked Data

ClinVar Variation Id: 330243
ClinVar RCV Id: RCV000297568
dbSNP Id: rs886054650
gnomAD v2: 19-5903929-A-G
gnomAD v3: 19-5903918-A-G
gnomAD v4: 19-5903918-A-G
MyVariant Identifiers: chr19:g.5903929A>G (hg19) chr19:g.5903918A>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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