Canonical Allele Identifier: CA405957284

Gene: COQ8B

Linked Data

• gnomAD v4: 19-40692060-C-A
• MyVariant Identifiers: chr19:g.41197965C>A (hg19) ; chr19:g.40692060C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40692060C>A , CM000681.2:g.40692060C>A	GRCh38
NC_000019.9:g.41197965C>A , CM000681.1:g.41197965C>A	GRCh37
NC_000019.8:g.45889805C>A	NCBI36
NG_027800.1:g.29826G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.1610G>T MANE Select	ENSP00000315118.3:p.Gly537Val
ENST00000593724.2:n.3433G>T
ENST00000594490.6:c.1532G>T	ENSP00000471310.2:p.Gly511Val
ENST00000594720.6:c.1610G>T	ENSP00000470876.2:p.Gly537Val
ENST00000596455.6:n.1902G>T
ENST00000601967.6:c.1610G>T	ENSP00000470916.2:p.Gly537Val
ENST00000676555.1:c.*1035G>T	ENSP00000503387.1:n.*1035G>T
ENST00000676578.1:c.*1352G>T	ENSP00000504076.1:n.*1352G>T
ENST00000676960.1:n.1735G>T
ENST00000676962.1:n.1889G>T
ENST00000677018.1:c.1610G>T	ENSP00000503480.1:p.Gly537Val
ENST00000677039.1:n.3813G>T
ENST00000677399.1:n.2052G>T
ENST00000677496.1:c.1283G>T	ENSP00000504773.1:p.Gly428Val
ENST00000677517.1:c.1283G>T	ENSP00000503519.1:p.Gly428Val
ENST00000677633.1:c.*1033G>T	ENSP00000503645.1:n.*1033G>T
ENST00000677800.1:c.*4714G>T	ENSP00000503794.1:n.*4714G>T
ENST00000678057.1:c.*1174G>T	ENSP00000503762.1:n.*1174G>T
ENST00000678119.1:n.1804G>T
ENST00000678166.1:n.1753G>T
ENST00000678312.1:n.1947G>T
ENST00000678316.1:c.*1033G>T	ENSP00000504112.1:n.*1033G>T
ENST00000678371.1:n.2060G>T
ENST00000678404.1:c.1610G>T	ENSP00000503944.1:p.Gly537Val
ENST00000678419.1:c.1610G>T	ENSP00000504085.1:p.Gly537Val
ENST00000678433.1:n.1966G>T
ENST00000678467.1:c.1610G>T	ENSP00000504072.1:p.Gly537Val
ENST00000678569.1:c.*595G>T	ENSP00000504261.1:n.*595G>T
ENST00000678961.1:n.1965G>T
ENST00000679002.1:n.1789G>T
ENST00000679012.1:c.1166G>T	ENSP00000504446.1:p.Gly389Val
ENST00000679070.1:c.*1029G>T	ENSP00000503759.1:n.*1029G>T
ENST00000679130.1:c.1610G>T	ENSP00000504845.1:p.Gly537Val
ENST00000679315.1:c.*1440G>T	ENSP00000503065.1:n.*1440G>T
ENST00000243583.10:c.1487G>T	ENSP00000243583.5:p.Gly496Val
ENST00000324464.7:c.1610G>T	ENSP00000315118.3:p.Gly537Val
ENST00000593724.1:n.1725G>T
NM_001142555.2:c.1487G>T	NP_001136027.1:p.Gly496Val
NM_024876.3:c.1610G>T	NP_079152.3:p.Gly537Val
XM_005259270.3:c.1772G>T	XP_005259327.2:p.Gly591Val
XM_005259271.3:c.1610G>T	XP_005259328.1:p.Gly537Val
XM_005259272.3:c.1610G>T	XP_005259329.1:p.Gly537Val
XM_005259273.3:c.1610G>T	XP_005259330.1:p.Gly537Val
XM_006723392.2:c.1610G>T	XP_006723455.1:p.Gly537Val
XM_006723393.2:c.1610G>T	XP_006723456.1:p.Gly537Val
XM_011527334.1:c.1610G>T	XP_011525636.1:p.Gly537Val
XM_011527335.1:c.1469G>T	XP_011525637.1:p.Gly490Val
XM_011527336.1:c.1640G>T	XP_011525638.1:p.Gly547Val
XM_011527337.1:c.1610G>T	XP_011525639.1:p.Gly537Val
XM_011527338.1:c.1610G>T	XP_011525640.1:p.Gly537Val
NM_024876.4:c.1610G>T MANE Select	NP_079152.3:p.Gly537Val
NM_001142555.3:c.1487G>T	NP_001136027.1:p.Gly496Val