Canonical Allele Identifier: CA1583356701
Gene: UQCRQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132868696A= , CM000667.2:g.132868696A= GRCh38
NC_000005.9:g.132204388A= , CM000667.1:g.132204388A= GRCh37
NC_000005.8:g.132232287A= NCBI36
NG_012221.1:g.7070A=
NG_047051.1:g.3189T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378670.8:c.*1114A= MANE Select ENSP00000367939.3:n.*1114A=
NM_014402.4:c.*1114A= NP_055217.2:n.*1114A=
NM_014402.5:c.*1114A= MANE Select NP_055217.2:n.*1114A=