Canonical Allele Identifier: CA405957754

Gene: COQ8B

Linked Data

• dbSNP Id: rs2081977576
• gnomAD v3: 19-40692270-T-C
• gnomAD v4: 19-40692270-T-C
• MyVariant Identifiers: chr19:g.41198175T>C (hg19) ; chr19:g.40692270T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40692270T>C , CM000681.2:g.40692270T>C	GRCh38
NC_000019.9:g.41198175T>C , CM000681.1:g.41198175T>C	GRCh37
NC_000019.8:g.45890015T>C	NCBI36
NG_027800.1:g.29616A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.1400A>G MANE Select	ENSP00000315118.3:p.Gln467Arg
ENST00000593724.2:n.3223A>G
ENST00000594490.6:c.1322A>G	ENSP00000471310.2:p.Gln441Arg
ENST00000594720.6:c.1400A>G	ENSP00000470876.2:p.Gln467Arg
ENST00000596455.6:n.1692A>G
ENST00000601967.6:c.1400A>G	ENSP00000470916.2:p.Gln467Arg
ENST00000676555.1:c.*825A>G	ENSP00000503387.1:n.*825A>G
ENST00000676578.1:c.*1142A>G	ENSP00000504076.1:n.*1142A>G
ENST00000676960.1:n.1525A>G
ENST00000676962.1:n.1679A>G
ENST00000677018.1:c.1400A>G	ENSP00000503480.1:p.Gln467Arg
ENST00000677039.1:n.3603A>G
ENST00000677399.1:n.1842A>G
ENST00000677496.1:c.1073A>G	ENSP00000504773.1:p.Gln358Arg
ENST00000677517.1:c.1073A>G	ENSP00000503519.1:p.Gln358Arg
ENST00000677633.1:c.*823A>G	ENSP00000503645.1:n.*823A>G
ENST00000677800.1:c.*4504A>G	ENSP00000503794.1:n.*4504A>G
ENST00000678057.1:c.*964A>G	ENSP00000503762.1:n.*964A>G
ENST00000678119.1:n.1594A>G
ENST00000678166.1:n.1543A>G
ENST00000678312.1:n.1737A>G
ENST00000678316.1:c.*823A>G	ENSP00000504112.1:n.*823A>G
ENST00000678371.1:n.1850A>G
ENST00000678404.1:c.1400A>G	ENSP00000503944.1:p.Gln467Arg
ENST00000678419.1:c.1400A>G	ENSP00000504085.1:p.Gln467Arg
ENST00000678433.1:n.1756A>G
ENST00000678467.1:c.1400A>G	ENSP00000504072.1:p.Gln467Arg
ENST00000678569.1:c.*385A>G	ENSP00000504261.1:n.*385A>G
ENST00000678961.1:n.1755A>G
ENST00000679002.1:n.1579A>G
ENST00000679012.1:c.956A>G	ENSP00000504446.1:p.Gln319Arg
ENST00000679070.1:c.*819A>G	ENSP00000503759.1:n.*819A>G
ENST00000679130.1:c.1400A>G	ENSP00000504845.1:p.Gln467Arg
ENST00000679315.1:c.*1230A>G	ENSP00000503065.1:n.*1230A>G
ENST00000243583.10:c.1277A>G	ENSP00000243583.5:p.Gln426Arg
ENST00000324464.7:c.1400A>G	ENSP00000315118.3:p.Gln467Arg
ENST00000593724.1:n.1515A>G
NM_001142555.2:c.1277A>G	NP_001136027.1:p.Gln426Arg
NM_024876.3:c.1400A>G	NP_079152.3:p.Gln467Arg
XM_005259270.3:c.1562A>G	XP_005259327.2:p.Gln521Arg
XM_005259271.3:c.1400A>G	XP_005259328.1:p.Gln467Arg
XM_005259272.3:c.1400A>G	XP_005259329.1:p.Gln467Arg
XM_005259273.3:c.1400A>G	XP_005259330.1:p.Gln467Arg
XM_006723392.2:c.1400A>G	XP_006723455.1:p.Gln467Arg
XM_006723393.2:c.1400A>G	XP_006723456.1:p.Gln467Arg
XM_011527334.1:c.1400A>G	XP_011525636.1:p.Gln467Arg
XM_011527335.1:c.1259A>G	XP_011525637.1:p.Gln420Arg
XM_011527336.1:c.1430A>G	XP_011525638.1:p.Gln477Arg
XM_011527337.1:c.1400A>G	XP_011525639.1:p.Gln467Arg
XM_011527338.1:c.1400A>G	XP_011525640.1:p.Gln467Arg
NM_024876.4:c.1400A>G MANE Select	NP_079152.3:p.Gln467Arg
NM_001142555.3:c.1277A>G	NP_001136027.1:p.Gln426Arg