Canonical Allele Identifier: CA804030110
Gene: UQCRQ HGNC NCBI

Linked Data

dbSNP Id: rs1256463214
MyVariant Identifiers: chr5:g.132204468A>G (hg19) chr5:g.132868776A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132868776A>G , CM000667.2:g.132868776A>G GRCh38
NC_000005.9:g.132204468A>G , CM000667.1:g.132204468A>G GRCh37
NC_000005.8:g.132232367A>G NCBI36
NG_012221.1:g.7150A>G
NG_047051.1:g.3109T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378670.8:c.*1194A>G MANE Select ENSP00000367939.3:n.*1194A>G
NM_014402.4:c.*1194A>G NP_055217.2:n.*1194A>G
NM_014402.5:c.*1194A>G MANE Select NP_055217.2:n.*1194A>G
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Search 100 bp 3'