Canonical Allele Identifier: CA2320171561
Gene: NDUFA11 HGNC NCBI

Linked Data

dbSNP Id: rs1443048708
gnomAD v4: 19-5903920-G-A
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Genomic Alleles

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

Transcript Alleles

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