Canonical Allele Identifier: CA1583356683
Gene: UQCRQ HGNC NCBI

Linked Data

dbSNP Id: rs1671112777
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132868663C>G , CM000667.2:g.132868663C>G GRCh38
NC_000005.9:g.132204355C>G , CM000667.1:g.132204355C>G GRCh37
NC_000005.8:g.132232254C>G NCBI36
NG_012221.1:g.7037C>G
NG_047051.1:g.3222G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378670.8:c.*1081C>G MANE Select ENSP00000367939.3:n.*1081C>G
NM_014402.4:c.*1081C>G NP_055217.2:n.*1081C>G
NM_014402.5:c.*1081C>G MANE Select NP_055217.2:n.*1081C>G
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