Canonical Allele Identifier: CA405963928

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41209650C>A (hg19) ; chr19:g.40703745C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40703745C>A , CM000681.2:g.40703745C>A	GRCh38
NC_000019.9:g.41209650C>A , CM000681.1:g.41209650C>A	GRCh37
NC_000019.8:g.45901490C>A	NCBI36
NG_027800.1:g.18141G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.687G>T MANE Select	ENSP00000315118.3:p.Arg229Ser
ENST00000593724.2:n.393-123G>T
ENST00000594490.6:c.609G>T	ENSP00000471310.2:p.Arg203Ser
ENST00000594720.6:c.687G>T	ENSP00000470876.2:p.Arg229Ser
ENST00000596455.6:n.979G>T
ENST00000601967.6:c.687G>T	ENSP00000470916.2:p.Arg229Ser
ENST00000676555.1:c.687G>T	ENSP00000503387.1:p.Arg229Ser
ENST00000676578.1:c.*429G>T	ENSP00000504076.1:n.*429G>T
ENST00000676960.1:n.812G>T
ENST00000676962.1:n.966G>T
ENST00000677018.1:c.687G>T	ENSP00000503480.1:p.Arg229Ser
ENST00000677039.1:n.742G>T
ENST00000677399.1:n.1129G>T
ENST00000677496.1:c.360G>T	ENSP00000504773.1:p.Arg120Ser
ENST00000677517.1:c.360G>T	ENSP00000503519.1:p.Arg120Ser
ENST00000677633.1:c.*110G>T	ENSP00000503645.1:n.*110G>T
ENST00000677800.1:c.*3791G>T	ENSP00000503794.1:n.*3791G>T
ENST00000678057.1:c.*251G>T	ENSP00000503762.1:n.*251G>T
ENST00000678119.1:n.881G>T
ENST00000678166.1:n.861-123G>T
ENST00000678312.1:n.1024G>T
ENST00000678316.1:c.*110G>T	ENSP00000504112.1:n.*110G>T
ENST00000678371.1:n.1045G>T
ENST00000678404.1:c.687G>T	ENSP00000503944.1:p.Arg229Ser
ENST00000678419.1:c.687G>T	ENSP00000504085.1:p.Arg229Ser
ENST00000678433.1:n.1047G>T
ENST00000678467.1:c.687G>T	ENSP00000504072.1:p.Arg229Ser
ENST00000678569.1:c.687G>T	ENSP00000504261.1:p.Arg229Ser
ENST00000678961.1:n.870G>T
ENST00000679002.1:n.866G>T
ENST00000679012.1:c.243G>T	ENSP00000504446.1:p.Arg81Ser
ENST00000679070.1:c.*110G>T	ENSP00000503759.1:n.*110G>T
ENST00000679130.1:c.687G>T	ENSP00000504845.1:p.Arg229Ser
ENST00000679315.1:c.*517G>T	ENSP00000503065.1:n.*517G>T
ENST00000243583.10:c.564G>T	ENSP00000243583.5:p.Arg188Ser
ENST00000324464.7:c.687G>T	ENSP00000315118.3:p.Arg229Ser
ENST00000595254.5:c.360G>T	ENSP00000470894.1:p.Arg120Ser
ENST00000596455.5:n.807G>T
ENST00000599643.5:c.336-123G>T	ENSP00000471192.1:n.336-123G>T
ENST00000601304.5:c.*461G>T	ENSP00000472519.1:n.*461G>T
ENST00000601967.5:c.687G>T	ENSP00000470916.1:p.Arg229Ser
NM_001142555.2:c.564G>T	NP_001136027.1:p.Arg188Ser
NM_024876.3:c.687G>T	NP_079152.3:p.Arg229Ser
XM_005259270.3:c.849G>T	XP_005259327.2:p.Arg283Ser
XM_005259271.3:c.687G>T	XP_005259328.1:p.Arg229Ser
XM_005259272.3:c.687G>T	XP_005259329.1:p.Arg229Ser
XM_005259273.3:c.687G>T	XP_005259330.1:p.Arg229Ser
XM_006723392.2:c.687G>T	XP_006723455.1:p.Arg229Ser
XM_006723393.2:c.687G>T	XP_006723456.1:p.Arg229Ser
XM_011527334.1:c.687G>T	XP_011525636.1:p.Arg229Ser
XM_011527335.1:c.577-123G>T	XP_011525637.1:n.577-123G>T
XM_011527336.1:c.717G>T	XP_011525638.1:p.Arg239Ser
XM_011527337.1:c.687G>T	XP_011525639.1:p.Arg229Ser
XM_011527338.1:c.687G>T	XP_011525640.1:p.Arg229Ser
NM_024876.4:c.687G>T MANE Select	NP_079152.3:p.Arg229Ser
NM_001142555.3:c.564G>T	NP_001136027.1:p.Arg188Ser