Canonical Allele Identifier: CA804030080
Gene: UQCRQ HGNC NCBI

Linked Data

dbSNP Id: rs1301957115
gnomAD v3: 5-132868700-A-T
gnomAD v4: 5-132868700-A-T
MyVariant Identifiers: chr5:g.132204392A>T (hg19) chr5:g.132868700A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132868700A>T , CM000667.2:g.132868700A>T GRCh38
NC_000005.9:g.132204392A>T , CM000667.1:g.132204392A>T GRCh37
NC_000005.8:g.132232291A>T NCBI36
NG_012221.1:g.7074A>T
NG_047051.1:g.3185T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378670.8:c.*1118A>T MANE Select ENSP00000367939.3:n.*1118A>T
NM_014402.4:c.*1118A>T NP_055217.2:n.*1118A>T
NM_014402.5:c.*1118A>T MANE Select NP_055217.2:n.*1118A>T
Search 100 bp 5'
Search 100 bp 3'