Canonical Allele Identifier: CA1583356778
Gene: UQCRQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132868827A= , CM000667.2:g.132868827A= GRCh38
NC_000005.9:g.132204519A= , CM000667.1:g.132204519A= GRCh37
NC_000005.8:g.132232418A= NCBI36
NG_012221.1:g.7201A=
NG_047051.1:g.3058T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378670.8:c.*1245A= MANE Select ENSP00000367939.3:n.*1245A=
NM_014402.4:c.*1245A= NP_055217.2:n.*1245A=
NM_014402.5:c.*1245A= MANE Select NP_055217.2:n.*1245A=