Canonical Allele Identifier: CA1583356702
Gene: UQCRQ HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132868697G= , CM000667.2:g.132868697G= GRCh38
NC_000005.9:g.132204389G= , CM000667.1:g.132204389G= GRCh37
NC_000005.8:g.132232288G= NCBI36
NG_012221.1:g.7071G=
NG_047051.1:g.3188C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378670.8:c.*1115G= MANE Select ENSP00000367939.3:n.*1115G=
NM_014402.4:c.*1115G= NP_055217.2:n.*1115G=
NM_014402.5:c.*1115G= MANE Select NP_055217.2:n.*1115G=
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