Canonical Allele Identifier: CA631619908
Gene: NDUFA11 HGNC NCBI

Linked Data

dbSNP Id: rs1215084114
gnomAD v2: 19-5903927-G-A
gnomAD v4: 19-5903916-G-A
MyVariant Identifiers: chr19:g.5903927G>A (hg19) chr19:g.5903916G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903916G>A , CM000681.2:g.5903916G>A GRCh38
NC_000019.9:g.5903927G>A , CM000681.1:g.5903927G>A GRCh37
NC_000019.8:g.5854927G>A NCBI36
NG_027808.1:g.5098C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000591160.1:n.91C>T
NM_001193375.1:c.-208C>T NP_001180304.1:n.-208C>T
NM_175614.4:c.-208C>T NP_783313.1:n.-208C>T
NR_034166.2:n.98C>T
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