Canonical Allele Identifier: CA1583356771
Gene: UQCRQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132868810T= , CM000667.2:g.132868810T= GRCh38
NC_000005.9:g.132204502T= , CM000667.1:g.132204502T= GRCh37
NC_000005.8:g.132232401T= NCBI36
NG_012221.1:g.7184T=
NG_047051.1:g.3075A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378670.8:c.*1228T= MANE Select ENSP00000367939.3:n.*1228T=
NM_014402.4:c.*1228T= NP_055217.2:n.*1228T=
NM_014402.5:c.*1228T= MANE Select NP_055217.2:n.*1228T=