Canonical Allele Identifier: CA631619909
Gene: NDUFA11 HGNC NCBI

Linked Data

dbSNP Id: rs1443048708
gnomAD v2: 19-5903931-G-T
gnomAD v4: 19-5903920-G-T
MyVariant Identifiers: chr19:g.5903931G>T (hg19) chr19:g.5903920G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5903920G>T , CM000681.2:g.5903920G>T GRCh38
NC_000019.9:g.5903931G>T , CM000681.1:g.5903931G>T GRCh37
NC_000019.8:g.5854931G>T NCBI36
NG_027808.1:g.5094C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000591160.1:n.87C>A
NM_001193375.1:c.-212C>A NP_001180304.1:n.-212C>A
NM_175614.4:c.-212C>A NP_783313.1:n.-212C>A
NR_034166.2:n.94C>A
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