Canonical Allele Identifier: CA405958072

Gene: COQ8B

Linked Data

• dbSNP Id: rs1197224740
• gnomAD v3: 19-40692349-C-T
• gnomAD v4: 19-40692349-C-T
• MyVariant Identifiers: chr19:g.41198254C>T (hg19) ; chr19:g.40692349C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40692349C>T , CM000681.2:g.40692349C>T	GRCh38
NC_000019.9:g.41198254C>T , CM000681.1:g.41198254C>T	GRCh37
NC_000019.8:g.45890094C>T	NCBI36
NG_027800.1:g.29537G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.1321G>A MANE Select	ENSP00000315118.3:p.Ala441Thr
ENST00000593724.2:n.3144G>A
ENST00000594490.6:c.1243G>A	ENSP00000471310.2:p.Ala415Thr
ENST00000594720.6:c.1321G>A	ENSP00000470876.2:p.Ala441Thr
ENST00000596455.6:n.1613G>A
ENST00000601967.6:c.1321G>A	ENSP00000470916.2:p.Ala441Thr
ENST00000676555.1:c.*746G>A	ENSP00000503387.1:n.*746G>A
ENST00000676578.1:c.*1063G>A	ENSP00000504076.1:n.*1063G>A
ENST00000676960.1:n.1446G>A
ENST00000676962.1:n.1600G>A
ENST00000677018.1:c.1321G>A	ENSP00000503480.1:p.Ala441Thr
ENST00000677039.1:n.3524G>A
ENST00000677399.1:n.1763G>A
ENST00000677496.1:c.994G>A	ENSP00000504773.1:p.Ala332Thr
ENST00000677517.1:c.994G>A	ENSP00000503519.1:p.Ala332Thr
ENST00000677633.1:c.*744G>A	ENSP00000503645.1:n.*744G>A
ENST00000677800.1:c.*4425G>A	ENSP00000503794.1:n.*4425G>A
ENST00000678057.1:c.*885G>A	ENSP00000503762.1:n.*885G>A
ENST00000678119.1:n.1515G>A
ENST00000678166.1:n.1464G>A
ENST00000678312.1:n.1658G>A
ENST00000678316.1:c.*744G>A	ENSP00000504112.1:n.*744G>A
ENST00000678371.1:n.1771G>A
ENST00000678404.1:c.1321G>A	ENSP00000503944.1:p.Ala441Thr
ENST00000678419.1:c.1321G>A	ENSP00000504085.1:p.Ala441Thr
ENST00000678433.1:n.1677G>A
ENST00000678467.1:c.1321G>A	ENSP00000504072.1:p.Ala441Thr
ENST00000678569.1:c.*306G>A	ENSP00000504261.1:n.*306G>A
ENST00000678961.1:n.1676G>A
ENST00000679002.1:n.1500G>A
ENST00000679012.1:c.877G>A	ENSP00000504446.1:p.Ala293Thr
ENST00000679070.1:c.*740G>A	ENSP00000503759.1:n.*740G>A
ENST00000679130.1:c.1321G>A	ENSP00000504845.1:p.Ala441Thr
ENST00000679315.1:c.*1151G>A	ENSP00000503065.1:n.*1151G>A
ENST00000243583.10:c.1198G>A	ENSP00000243583.5:p.Ala400Thr
ENST00000324464.7:c.1321G>A	ENSP00000315118.3:p.Ala441Thr
ENST00000593724.1:n.1436G>A
NM_001142555.2:c.1198G>A	NP_001136027.1:p.Ala400Thr
NM_024876.3:c.1321G>A	NP_079152.3:p.Ala441Thr
XM_005259270.3:c.1483G>A	XP_005259327.2:p.Ala495Thr
XM_005259271.3:c.1321G>A	XP_005259328.1:p.Ala441Thr
XM_005259272.3:c.1321G>A	XP_005259329.1:p.Ala441Thr
XM_005259273.3:c.1321G>A	XP_005259330.1:p.Ala441Thr
XM_006723392.2:c.1321G>A	XP_006723455.1:p.Ala441Thr
XM_006723393.2:c.1321G>A	XP_006723456.1:p.Ala441Thr
XM_011527334.1:c.1321G>A	XP_011525636.1:p.Ala441Thr
XM_011527335.1:c.1180G>A	XP_011525637.1:p.Ala394Thr
XM_011527336.1:c.1351G>A	XP_011525638.1:p.Ala451Thr
XM_011527337.1:c.1321G>A	XP_011525639.1:p.Ala441Thr
XM_011527338.1:c.1321G>A	XP_011525640.1:p.Ala441Thr
NM_024876.4:c.1321G>A MANE Select	NP_079152.3:p.Ala441Thr
NM_001142555.3:c.1198G>A	NP_001136027.1:p.Ala400Thr