Canonical Allele Identifier: CA9119075
Gene: NDUFA11 HGNC NCBI

Linked Data

dbSNP Id: rs765494078
ExAC: 19:5903826 G / A
gnomAD v2: 19-5903826-G-A
gnomAD v3: 19-5903815-G-A
gnomAD v4: 19-5903815-G-A
MyVariant Identifiers: chr19:g.5903826G>A (hg19) chr19:g.5903815G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903815G>A , CM000681.2:g.5903815G>A GRCh38
NC_000019.9:g.5903826G>A , CM000681.1:g.5903826G>A GRCh37
NC_000019.8:g.5854826G>A NCBI36
NG_027808.1:g.5199C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000591160.1:n.192C>T
NM_001193375.1:c.-107C>T NP_001180304.1:n.-107C>T
NM_175614.4:c.-107C>T NP_783313.1:n.-107C>T
NR_034166.2:n.199C>T
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