Canonical Allele Identifier: CA2336101882
Gene: COQ8B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40691783C= , CM000681.2:g.40691783C= GRCh38
NC_000019.9:g.41197688C= , CM000681.1:g.41197688C= GRCh37
NC_000019.8:g.45889528C= NCBI36
NG_027800.1:g.30103G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324464.8:c.*252G= MANE Select ENSP00000315118.3:n.*252G=
ENST00000593724.2:n.3710G=
ENST00000594490.6:c.*252G= ENSP00000471310.2:n.*252G=
ENST00000594720.6:c.*252G= ENSP00000470876.2:n.*252G=
ENST00000596455.6:n.2179G=
ENST00000601967.6:c.*252G= ENSP00000470916.2:n.*252G=
ENST00000676555.1:c.*1312G= ENSP00000503387.1:n.*1312G=
ENST00000676578.1:c.*1629G= ENSP00000504076.1:n.*1629G=
ENST00000676960.1:n.2012G=
ENST00000676962.1:n.2166G=
ENST00000677018.1:c.*252G= ENSP00000503480.1:n.*252G=
ENST00000677039.1:n.4090G=
ENST00000677399.1:n.2329G=
ENST00000677496.1:c.*252G= ENSP00000504773.1:n.*252G=
ENST00000677517.1:c.*252G= ENSP00000503519.1:n.*252G=
ENST00000677633.1:c.*1310G= ENSP00000503645.1:n.*1310G=
ENST00000677800.1:c.*4991G= ENSP00000503794.1:n.*4991G=
ENST00000678057.1:c.*1451G= ENSP00000503762.1:n.*1451G=
ENST00000678119.1:n.2081G=
ENST00000678166.1:n.2030G=
ENST00000678312.1:n.2224G=
ENST00000678316.1:c.*1310G= ENSP00000504112.1:n.*1310G=
ENST00000678371.1:n.2337G=
ENST00000678404.1:c.*252G= ENSP00000503944.1:n.*252G=
ENST00000678419.1:c.*252G= ENSP00000504085.1:n.*252G=
ENST00000678433.1:n.2243G=
ENST00000678467.1:c.*252G= ENSP00000504072.1:n.*252G=
ENST00000678569.1:c.*872G= ENSP00000504261.1:n.*872G=
ENST00000678961.1:n.2242G=
ENST00000679002.1:n.2066G=
ENST00000679012.1:c.*252G= ENSP00000504446.1:n.*252G=
ENST00000679070.1:c.*1306G= ENSP00000503759.1:n.*1306G=
ENST00000679130.1:c.*252G= ENSP00000504845.1:n.*252G=
ENST00000679315.1:c.*1717G= ENSP00000503065.1:n.*1717G=
ENST00000243583.10:c.*252G= ENSP00000243583.5:n.*252G=
ENST00000324464.7:c.*252G= ENSP00000315118.3:n.*252G=
ENST00000593724.1:n.2002G=
NM_001142555.2:c.*252G= NP_001136027.1:n.*252G=
NM_024876.3:c.*252G= NP_079152.3:n.*252G=
XM_005259270.3:c.*252G= XP_005259327.2:n.*252G=
XM_005259271.3:c.*252G= XP_005259328.1:n.*252G=
XM_005259272.3:c.*252G= XP_005259329.1:n.*252G=
XM_005259273.3:c.*252G= XP_005259330.1:n.*252G=
XM_006723392.2:c.*252G= XP_006723455.1:n.*252G=
XM_006723393.2:c.*252G= XP_006723456.1:n.*252G=
XM_011527334.1:c.*252G= XP_011525636.1:n.*252G=
XM_011527335.1:c.*252G= XP_011525637.1:n.*252G=
XM_011527336.1:c.*252G= XP_011525638.1:n.*252G=
XM_011527337.1:c.*252G= XP_011525639.1:n.*252G=
XM_011527338.1:c.*252G= XP_011525640.1:n.*252G=
NM_024876.4:c.*252G= MANE Select NP_079152.3:n.*252G=
NM_001142555.3:c.*252G= NP_001136027.1:n.*252G=