Canonical Allele Identifier: CA405957766

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41198178A>C (hg19) ; chr19:g.40692273A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40692273A>C , CM000681.2:g.40692273A>C	GRCh38
NC_000019.9:g.41198178A>C , CM000681.1:g.41198178A>C	GRCh37
NC_000019.8:g.45890018A>C	NCBI36
NG_027800.1:g.29613T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.1397T>G MANE Select	ENSP00000315118.3:p.Ile466Arg
ENST00000593724.2:n.3220T>G
ENST00000594490.6:c.1319T>G	ENSP00000471310.2:p.Ile440Arg
ENST00000594720.6:c.1397T>G	ENSP00000470876.2:p.Ile466Arg
ENST00000596455.6:n.1689T>G
ENST00000601967.6:c.1397T>G	ENSP00000470916.2:p.Ile466Arg
ENST00000676555.1:c.*822T>G	ENSP00000503387.1:n.*822T>G
ENST00000676578.1:c.*1139T>G	ENSP00000504076.1:n.*1139T>G
ENST00000676960.1:n.1522T>G
ENST00000676962.1:n.1676T>G
ENST00000677018.1:c.1397T>G	ENSP00000503480.1:p.Ile466Arg
ENST00000677039.1:n.3600T>G
ENST00000677399.1:n.1839T>G
ENST00000677496.1:c.1070T>G	ENSP00000504773.1:p.Ile357Arg
ENST00000677517.1:c.1070T>G	ENSP00000503519.1:p.Ile357Arg
ENST00000677633.1:c.*820T>G	ENSP00000503645.1:n.*820T>G
ENST00000677800.1:c.*4501T>G	ENSP00000503794.1:n.*4501T>G
ENST00000678057.1:c.*961T>G	ENSP00000503762.1:n.*961T>G
ENST00000678119.1:n.1591T>G
ENST00000678166.1:n.1540T>G
ENST00000678312.1:n.1734T>G
ENST00000678316.1:c.*820T>G	ENSP00000504112.1:n.*820T>G
ENST00000678371.1:n.1847T>G
ENST00000678404.1:c.1397T>G	ENSP00000503944.1:p.Ile466Arg
ENST00000678419.1:c.1397T>G	ENSP00000504085.1:p.Ile466Arg
ENST00000678433.1:n.1753T>G
ENST00000678467.1:c.1397T>G	ENSP00000504072.1:p.Ile466Arg
ENST00000678569.1:c.*382T>G	ENSP00000504261.1:n.*382T>G
ENST00000678961.1:n.1752T>G
ENST00000679002.1:n.1576T>G
ENST00000679012.1:c.953T>G	ENSP00000504446.1:p.Ile318Arg
ENST00000679070.1:c.*816T>G	ENSP00000503759.1:n.*816T>G
ENST00000679130.1:c.1397T>G	ENSP00000504845.1:p.Ile466Arg
ENST00000679315.1:c.*1227T>G	ENSP00000503065.1:n.*1227T>G
ENST00000243583.10:c.1274T>G	ENSP00000243583.5:p.Ile425Arg
ENST00000324464.7:c.1397T>G	ENSP00000315118.3:p.Ile466Arg
ENST00000593724.1:n.1512T>G
NM_001142555.2:c.1274T>G	NP_001136027.1:p.Ile425Arg
NM_024876.3:c.1397T>G	NP_079152.3:p.Ile466Arg
XM_005259270.3:c.1559T>G	XP_005259327.2:p.Ile520Arg
XM_005259271.3:c.1397T>G	XP_005259328.1:p.Ile466Arg
XM_005259272.3:c.1397T>G	XP_005259329.1:p.Ile466Arg
XM_005259273.3:c.1397T>G	XP_005259330.1:p.Ile466Arg
XM_006723392.2:c.1397T>G	XP_006723455.1:p.Ile466Arg
XM_006723393.2:c.1397T>G	XP_006723456.1:p.Ile466Arg
XM_011527334.1:c.1397T>G	XP_011525636.1:p.Ile466Arg
XM_011527335.1:c.1256T>G	XP_011525637.1:p.Ile419Arg
XM_011527336.1:c.1427T>G	XP_011525638.1:p.Ile476Arg
XM_011527337.1:c.1397T>G	XP_011525639.1:p.Ile466Arg
XM_011527338.1:c.1397T>G	XP_011525640.1:p.Ile466Arg
NM_024876.4:c.1397T>G MANE Select	NP_079152.3:p.Ile466Arg
NM_001142555.3:c.1274T>G	NP_001136027.1:p.Ile425Arg