Canonical Allele Identifier: CA9450380

Gene: COQ8B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40705151T>C , CM000681.2:g.40705151T>C	GRCh38
NC_000019.9:g.41211056T>C , CM000681.1:g.41211056T>C	GRCh37
NC_000019.8:g.45902896T>C	NCBI36
NG_027800.1:g.16735A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.521A>G MANE Select	ENSP00000315118.3:p.His174Arg
ENST00000593724.2:n.393-1529A>G
ENST00000594490.6:c.443A>G	ENSP00000471310.2:p.His148Arg
ENST00000594720.6:c.521A>G	ENSP00000470876.2:p.His174Arg
ENST00000596455.6:n.813A>G
ENST00000601967.6:c.521A>G	ENSP00000470916.2:p.His174Arg
ENST00000676555.1:c.521A>G	ENSP00000503387.1:p.His174Arg
ENST00000676578.1:c.*263A>G	ENSP00000504076.1:n.*263A>G
ENST00000676960.1:n.646A>G
ENST00000676962.1:n.800A>G
ENST00000677018.1:c.521A>G	ENSP00000503480.1:p.His174Arg
ENST00000677039.1:n.576A>G
ENST00000677399.1:n.963A>G
ENST00000677496.1:c.194A>G	ENSP00000504773.1:p.His65Arg
ENST00000677517.1:c.194A>G	ENSP00000503519.1:p.His65Arg
ENST00000677633.1:c.514A>G	ENSP00000503645.1:p.Thr172Ala
ENST00000677800.1:c.*3625A>G	ENSP00000503794.1:n.*3625A>G
ENST00000678057.1:c.*85A>G	ENSP00000503762.1:n.*85A>G
ENST00000678119.1:n.715A>G
ENST00000678166.1:n.805A>G
ENST00000678312.1:n.858A>G
ENST00000678316.1:c.496A>G	ENSP00000504112.1:p.Thr166Ala
ENST00000678371.1:n.879A>G
ENST00000678404.1:c.521A>G	ENSP00000503944.1:p.His174Arg
ENST00000678419.1:c.521A>G	ENSP00000504085.1:p.His174Arg
ENST00000678433.1:n.881A>G
ENST00000678467.1:c.521A>G	ENSP00000504072.1:p.His174Arg
ENST00000678569.1:c.521A>G	ENSP00000504261.1:p.His174Arg
ENST00000678961.1:n.704A>G
ENST00000679002.1:n.700A>G
ENST00000679012.1:c.77A>G	ENSP00000504446.1:p.His26Arg
ENST00000679070.1:c.187A>G	ENSP00000503759.1:p.Thr63Ala
ENST00000679130.1:c.521A>G	ENSP00000504845.1:p.His174Arg
ENST00000679315.1:c.*351A>G	ENSP00000503065.1:n.*351A>G
ENST00000243583.10:c.398A>G	ENSP00000243583.5:p.His133Arg
ENST00000324464.7:c.521A>G	ENSP00000315118.3:p.His174Arg
ENST00000595254.5:c.194A>G	ENSP00000470894.1:p.His65Arg
ENST00000596455.5:n.641A>G
ENST00000599643.5:c.280A>G	ENSP00000471192.1:p.Thr94Ala
ENST00000600080.5:c.187A>G	ENSP00000473017.1:p.Thr63Ala
ENST00000601304.5:c.*295A>G	ENSP00000472519.1:n.*295A>G
ENST00000601451.5:n.966A>G
ENST00000601967.5:c.521A>G	ENSP00000470916.1:p.His174Arg
NM_001142555.2:c.398A>G	NP_001136027.1:p.His133Arg
NM_024876.3:c.521A>G	NP_079152.3:p.His174Arg
XM_005259270.3:c.683A>G	XP_005259327.2:p.His228Arg
XM_005259271.3:c.521A>G	XP_005259328.1:p.His174Arg
XM_005259272.3:c.521A>G	XP_005259329.1:p.His174Arg
XM_005259273.3:c.521A>G	XP_005259330.1:p.His174Arg
XM_006723392.2:c.521A>G	XP_006723455.1:p.His174Arg
XM_006723393.2:c.521A>G	XP_006723456.1:p.His174Arg
XM_011527334.1:c.521A>G	XP_011525636.1:p.His174Arg
XM_011527335.1:c.521A>G	XP_011525637.1:p.His174Arg
XM_011527336.1:c.551A>G	XP_011525638.1:p.His184Arg
XM_011527337.1:c.521A>G	XP_011525639.1:p.His174Arg
XM_011527338.1:c.521A>G	XP_011525640.1:p.His174Arg
NM_024876.4:c.521A>G MANE Select	NP_079152.3:p.His174Arg
NM_001142555.3:c.398A>G	NP_001136027.1:p.His133Arg