Canonical Allele Identifier: CA405960696

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41206235T>G (hg19) ; chr19:g.40700330T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40700330T>G , CM000681.2:g.40700330T>G	GRCh38
NC_000019.9:g.41206235T>G , CM000681.1:g.41206235T>G	GRCh37
NC_000019.8:g.45898075T>G	NCBI36
NG_027800.1:g.21556A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.1015A>C MANE Select	ENSP00000315118.3:p.Ser339Arg
ENST00000593724.2:n.2838A>C
ENST00000594490.6:c.937A>C	ENSP00000471310.2:p.Ser313Arg
ENST00000594720.6:c.1015A>C	ENSP00000470876.2:p.Ser339Arg
ENST00000596455.6:n.1307A>C
ENST00000601967.6:c.1015A>C	ENSP00000470916.2:p.Ser339Arg
ENST00000676555.1:c.1015A>C	ENSP00000503387.1:p.Ser339Arg
ENST00000676578.1:c.*757A>C	ENSP00000504076.1:n.*757A>C
ENST00000676960.1:n.1140A>C
ENST00000676962.1:n.1294A>C
ENST00000677018.1:c.1015A>C	ENSP00000503480.1:p.Ser339Arg
ENST00000677039.1:n.3218A>C
ENST00000677399.1:n.1457A>C
ENST00000677496.1:c.688A>C	ENSP00000504773.1:p.Ser230Arg
ENST00000677517.1:c.688A>C	ENSP00000503519.1:p.Ser230Arg
ENST00000677633.1:c.*438A>C	ENSP00000503645.1:n.*438A>C
ENST00000677800.1:c.*4119A>C	ENSP00000503794.1:n.*4119A>C
ENST00000678057.1:c.*579A>C	ENSP00000503762.1:n.*579A>C
ENST00000678119.1:n.1209A>C
ENST00000678166.1:n.1158A>C
ENST00000678312.1:n.1352A>C
ENST00000678316.1:c.*438A>C	ENSP00000504112.1:n.*438A>C
ENST00000678371.1:n.1465A>C
ENST00000678404.1:c.1015A>C	ENSP00000503944.1:p.Ser339Arg
ENST00000678419.1:c.1015A>C	ENSP00000504085.1:p.Ser339Arg
ENST00000678433.1:n.1371A>C
ENST00000678467.1:c.1015A>C	ENSP00000504072.1:p.Ser339Arg
ENST00000678569.1:c.1011A>C	ENSP00000504261.1:p.Ter337Tyr
ENST00000678961.1:n.1370A>C
ENST00000679002.1:n.1194A>C
ENST00000679012.1:c.571A>C	ENSP00000504446.1:p.Ser191Arg
ENST00000679070.1:c.*434A>C	ENSP00000503759.1:n.*434A>C
ENST00000679130.1:c.1015A>C	ENSP00000504845.1:p.Ser339Arg
ENST00000679315.1:c.*845A>C	ENSP00000503065.1:n.*845A>C
ENST00000243583.10:c.892A>C	ENSP00000243583.5:p.Ser298Arg
ENST00000324464.7:c.1015A>C	ENSP00000315118.3:p.Ser339Arg
ENST00000593724.1:n.1130A>C
NM_001142555.2:c.892A>C	NP_001136027.1:p.Ser298Arg
NM_024876.3:c.1015A>C	NP_079152.3:p.Ser339Arg
XM_005259270.3:c.1177A>C	XP_005259327.2:p.Ser393Arg
XM_005259271.3:c.1015A>C	XP_005259328.1:p.Ser339Arg
XM_005259272.3:c.1015A>C	XP_005259329.1:p.Ser339Arg
XM_005259273.3:c.1015A>C	XP_005259330.1:p.Ser339Arg
XM_006723392.2:c.1015A>C	XP_006723455.1:p.Ser339Arg
XM_006723393.2:c.1015A>C	XP_006723456.1:p.Ser339Arg
XM_011527334.1:c.1015A>C	XP_011525636.1:p.Ser339Arg
XM_011527335.1:c.874A>C	XP_011525637.1:p.Ser292Arg
XM_011527336.1:c.1045A>C	XP_011525638.1:p.Ser349Arg
XM_011527337.1:c.1015A>C	XP_011525639.1:p.Ser339Arg
XM_011527338.1:c.1015A>C	XP_011525640.1:p.Ser339Arg
NM_024876.4:c.1015A>C MANE Select	NP_079152.3:p.Ser339Arg
NM_001142555.3:c.892A>C	NP_001136027.1:p.Ser298Arg