Canonical Allele Identifier: CA405960854

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41206283C>T (hg19) ; chr19:g.40700378C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40700378C>T , CM000681.2:g.40700378C>T	GRCh38
NC_000019.9:g.41206283C>T , CM000681.1:g.41206283C>T	GRCh37
NC_000019.8:g.45898123C>T	NCBI36
NG_027800.1:g.21508G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.967G>A MANE Select	ENSP00000315118.3:p.Gly323Ser
ENST00000593724.2:n.2790G>A
ENST00000594490.6:c.889G>A	ENSP00000471310.2:p.Gly297Ser
ENST00000594720.6:c.967G>A	ENSP00000470876.2:p.Gly323Ser
ENST00000596455.6:n.1259G>A
ENST00000601967.6:c.967G>A	ENSP00000470916.2:p.Gly323Ser
ENST00000676555.1:c.967G>A	ENSP00000503387.1:p.Gly323Ser
ENST00000676578.1:c.*709G>A	ENSP00000504076.1:n.*709G>A
ENST00000676960.1:n.1092G>A
ENST00000676962.1:n.1246G>A
ENST00000677018.1:c.967G>A	ENSP00000503480.1:p.Gly323Ser
ENST00000677039.1:n.3170G>A
ENST00000677399.1:n.1409G>A
ENST00000677496.1:c.640G>A	ENSP00000504773.1:p.Gly214Ser
ENST00000677517.1:c.640G>A	ENSP00000503519.1:p.Gly214Ser
ENST00000677633.1:c.*390G>A	ENSP00000503645.1:n.*390G>A
ENST00000677800.1:c.*4071G>A	ENSP00000503794.1:n.*4071G>A
ENST00000678057.1:c.*531G>A	ENSP00000503762.1:n.*531G>A
ENST00000678119.1:n.1161G>A
ENST00000678166.1:n.1110G>A
ENST00000678312.1:n.1304G>A
ENST00000678316.1:c.*390G>A	ENSP00000504112.1:n.*390G>A
ENST00000678371.1:n.1417G>A
ENST00000678404.1:c.967G>A	ENSP00000503944.1:p.Gly323Ser
ENST00000678419.1:c.967G>A	ENSP00000504085.1:p.Gly323Ser
ENST00000678433.1:n.1323G>A
ENST00000678467.1:c.967G>A	ENSP00000504072.1:p.Gly323Ser
ENST00000678569.1:c.963G>A	ENSP00000504261.1:p.Trp321Ter
ENST00000678961.1:n.1322G>A
ENST00000679002.1:n.1146G>A
ENST00000679012.1:c.523G>A	ENSP00000504446.1:p.Gly175Ser
ENST00000679070.1:c.*386G>A	ENSP00000503759.1:n.*386G>A
ENST00000679130.1:c.967G>A	ENSP00000504845.1:p.Gly323Ser
ENST00000679315.1:c.*797G>A	ENSP00000503065.1:n.*797G>A
ENST00000243583.10:c.844G>A	ENSP00000243583.5:p.Gly282Ser
ENST00000324464.7:c.967G>A	ENSP00000315118.3:p.Gly323Ser
ENST00000593724.1:n.1082G>A
NM_001142555.2:c.844G>A	NP_001136027.1:p.Gly282Ser
NM_024876.3:c.967G>A	NP_079152.3:p.Gly323Ser
XM_005259270.3:c.1129G>A	XP_005259327.2:p.Gly377Ser
XM_005259271.3:c.967G>A	XP_005259328.1:p.Gly323Ser
XM_005259272.3:c.967G>A	XP_005259329.1:p.Gly323Ser
XM_005259273.3:c.967G>A	XP_005259330.1:p.Gly323Ser
XM_006723392.2:c.967G>A	XP_006723455.1:p.Gly323Ser
XM_006723393.2:c.967G>A	XP_006723456.1:p.Gly323Ser
XM_011527334.1:c.967G>A	XP_011525636.1:p.Gly323Ser
XM_011527335.1:c.826G>A	XP_011525637.1:p.Gly276Ser
XM_011527336.1:c.997G>A	XP_011525638.1:p.Gly333Ser
XM_011527337.1:c.967G>A	XP_011525639.1:p.Gly323Ser
XM_011527338.1:c.967G>A	XP_011525640.1:p.Gly323Ser
NM_024876.4:c.967G>A MANE Select	NP_079152.3:p.Gly323Ser
NM_001142555.3:c.844G>A	NP_001136027.1:p.Gly282Ser