Canonical Allele Identifier: CA1583356745
Gene: UQCRQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132868758A= , CM000667.2:g.132868758A= GRCh38
NC_000005.9:g.132204450A= , CM000667.1:g.132204450A= GRCh37
NC_000005.8:g.132232349A= NCBI36
NG_012221.1:g.7132A=
NG_047051.1:g.3127T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378670.8:c.*1176A= MANE Select ENSP00000367939.3:n.*1176A=
NM_014402.4:c.*1176A= NP_055217.2:n.*1176A=
NM_014402.5:c.*1176A= MANE Select NP_055217.2:n.*1176A=