Canonical Allele Identifier: CA15360921
Gene: UQCRQ HGNC NCBI

Linked Data

ClinVar Variation Id: 905152
ClinVar RCV Id: RCV001153504
dbSNP Id: rs254284
gnomAD v2: 5-132204467-A-G
gnomAD v3: 5-132868775-A-G
gnomAD v4: 5-132868775-A-G
MyVariant Identifiers: chr5:g.132204467A>G (hg19) chr5:g.132868775A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132868775A>G , CM000667.2:g.132868775A>G GRCh38
NC_000005.9:g.132204467A>G , CM000667.1:g.132204467A>G GRCh37
NC_000005.8:g.132232366A>G NCBI36
NG_012221.1:g.7149A>G
NG_047051.1:g.3110T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378670.8:c.*1193A>G MANE Select ENSP00000367939.3:n.*1193A>G
NM_014402.4:c.*1193A>G NP_055217.2:n.*1193A>G
NM_014402.5:c.*1193A>G MANE Select NP_055217.2:n.*1193A>G
Search 100 bp 5'
Search 100 bp 3'