Canonical Allele Identifier: CA2320171557
Gene: NDUFA11 HGNC NCBI

Linked Data

dbSNP Id: rs1599698999
gnomAD v4: 19-5903914-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903914T>G , CM000681.2:g.5903914T>G GRCh38
NC_000019.9:g.5903925T>G , CM000681.1:g.5903925T>G GRCh37
NC_000019.8:g.5854925T>G NCBI36
NG_027808.1:g.5100A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000591160.1:n.93A>C
NM_001193375.1:c.-206A>C NP_001180304.1:n.-206A>C
NM_175614.4:c.-206A>C NP_783313.1:n.-206A>C
NR_034166.2:n.100A>C
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