Canonical Allele Identifier: CA405957398

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41198019T>C (hg19) ; chr19:g.40692114T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40692114T>C , CM000681.2:g.40692114T>C	GRCh38
NC_000019.9:g.41198019T>C , CM000681.1:g.41198019T>C	GRCh37
NC_000019.8:g.45889859T>C	NCBI36
NG_027800.1:g.29772A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.1556A>G MANE Select	ENSP00000315118.3:p.Tyr519Cys
ENST00000593724.2:n.3379A>G
ENST00000594490.6:c.1478A>G	ENSP00000471310.2:p.Tyr493Cys
ENST00000594720.6:c.1556A>G	ENSP00000470876.2:p.Tyr519Cys
ENST00000596455.6:n.1848A>G
ENST00000601967.6:c.1556A>G	ENSP00000470916.2:p.Tyr519Cys
ENST00000676555.1:c.*981A>G	ENSP00000503387.1:n.*981A>G
ENST00000676578.1:c.*1298A>G	ENSP00000504076.1:n.*1298A>G
ENST00000676960.1:n.1681A>G
ENST00000676962.1:n.1835A>G
ENST00000677018.1:c.1556A>G	ENSP00000503480.1:p.Tyr519Cys
ENST00000677039.1:n.3759A>G
ENST00000677399.1:n.1998A>G
ENST00000677496.1:c.1229A>G	ENSP00000504773.1:p.Tyr410Cys
ENST00000677517.1:c.1229A>G	ENSP00000503519.1:p.Tyr410Cys
ENST00000677633.1:c.*979A>G	ENSP00000503645.1:n.*979A>G
ENST00000677800.1:c.*4660A>G	ENSP00000503794.1:n.*4660A>G
ENST00000678057.1:c.*1120A>G	ENSP00000503762.1:n.*1120A>G
ENST00000678119.1:n.1750A>G
ENST00000678166.1:n.1699A>G
ENST00000678312.1:n.1893A>G
ENST00000678316.1:c.*979A>G	ENSP00000504112.1:n.*979A>G
ENST00000678371.1:n.2006A>G
ENST00000678404.1:c.1556A>G	ENSP00000503944.1:p.Tyr519Cys
ENST00000678419.1:c.1556A>G	ENSP00000504085.1:p.Tyr519Cys
ENST00000678433.1:n.1912A>G
ENST00000678467.1:c.1556A>G	ENSP00000504072.1:p.Tyr519Cys
ENST00000678569.1:c.*541A>G	ENSP00000504261.1:n.*541A>G
ENST00000678961.1:n.1911A>G
ENST00000679002.1:n.1735A>G
ENST00000679012.1:c.1112A>G	ENSP00000504446.1:p.Tyr371Cys
ENST00000679070.1:c.*975A>G	ENSP00000503759.1:n.*975A>G
ENST00000679130.1:c.1556A>G	ENSP00000504845.1:p.Tyr519Cys
ENST00000679315.1:c.*1386A>G	ENSP00000503065.1:n.*1386A>G
ENST00000243583.10:c.1433A>G	ENSP00000243583.5:p.Tyr478Cys
ENST00000324464.7:c.1556A>G	ENSP00000315118.3:p.Tyr519Cys
ENST00000593724.1:n.1671A>G
NM_001142555.2:c.1433A>G	NP_001136027.1:p.Tyr478Cys
NM_024876.3:c.1556A>G	NP_079152.3:p.Tyr519Cys
XM_005259270.3:c.1718A>G	XP_005259327.2:p.Tyr573Cys
XM_005259271.3:c.1556A>G	XP_005259328.1:p.Tyr519Cys
XM_005259272.3:c.1556A>G	XP_005259329.1:p.Tyr519Cys
XM_005259273.3:c.1556A>G	XP_005259330.1:p.Tyr519Cys
XM_006723392.2:c.1556A>G	XP_006723455.1:p.Tyr519Cys
XM_006723393.2:c.1556A>G	XP_006723456.1:p.Tyr519Cys
XM_011527334.1:c.1556A>G	XP_011525636.1:p.Tyr519Cys
XM_011527335.1:c.1415A>G	XP_011525637.1:p.Tyr472Cys
XM_011527336.1:c.1586A>G	XP_011525638.1:p.Tyr529Cys
XM_011527337.1:c.1556A>G	XP_011525639.1:p.Tyr519Cys
XM_011527338.1:c.1556A>G	XP_011525640.1:p.Tyr519Cys
NM_024876.4:c.1556A>G MANE Select	NP_079152.3:p.Tyr519Cys
NM_001142555.3:c.1433A>G	NP_001136027.1:p.Tyr478Cys