Canonical Allele Identifier: CA804030100
Gene: UQCRQ HGNC NCBI

Linked Data

dbSNP Id: rs1479635935
gnomAD v3: 5-132868758-A-C
gnomAD v4: 5-132868758-A-C
MyVariant Identifiers: chr5:g.132204450A>C (hg19) chr5:g.132868758A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132868758A>C , CM000667.2:g.132868758A>C GRCh38
NC_000005.9:g.132204450A>C , CM000667.1:g.132204450A>C GRCh37
NC_000005.8:g.132232349A>C NCBI36
NG_012221.1:g.7132A>C
NG_047051.1:g.3127T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378670.8:c.*1176A>C MANE Select ENSP00000367939.3:n.*1176A>C
NM_014402.4:c.*1176A>C NP_055217.2:n.*1176A>C
NM_014402.5:c.*1176A>C MANE Select NP_055217.2:n.*1176A>C
Search 100 bp 5'
Search 100 bp 3'