Canonical Allele Identifier: CA405957875

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41198207G>C (hg19) ; chr19:g.40692302G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40692302G>C , CM000681.2:g.40692302G>C	GRCh38
NC_000019.9:g.41198207G>C , CM000681.1:g.41198207G>C	GRCh37
NC_000019.8:g.45890047G>C	NCBI36
NG_027800.1:g.29584C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.1368C>G MANE Select	ENSP00000315118.3:p.Asp456Glu
ENST00000593724.2:n.3191C>G
ENST00000594490.6:c.1290C>G	ENSP00000471310.2:p.Asp430Glu
ENST00000594720.6:c.1368C>G	ENSP00000470876.2:p.Asp456Glu
ENST00000596455.6:n.1660C>G
ENST00000601967.6:c.1368C>G	ENSP00000470916.2:p.Asp456Glu
ENST00000676555.1:c.*793C>G	ENSP00000503387.1:n.*793C>G
ENST00000676578.1:c.*1110C>G	ENSP00000504076.1:n.*1110C>G
ENST00000676960.1:n.1493C>G
ENST00000676962.1:n.1647C>G
ENST00000677018.1:c.1368C>G	ENSP00000503480.1:p.Asp456Glu
ENST00000677039.1:n.3571C>G
ENST00000677399.1:n.1810C>G
ENST00000677496.1:c.1041C>G	ENSP00000504773.1:p.Asp347Glu
ENST00000677517.1:c.1041C>G	ENSP00000503519.1:p.Asp347Glu
ENST00000677633.1:c.*791C>G	ENSP00000503645.1:n.*791C>G
ENST00000677800.1:c.*4472C>G	ENSP00000503794.1:n.*4472C>G
ENST00000678057.1:c.*932C>G	ENSP00000503762.1:n.*932C>G
ENST00000678119.1:n.1562C>G
ENST00000678166.1:n.1511C>G
ENST00000678312.1:n.1705C>G
ENST00000678316.1:c.*791C>G	ENSP00000504112.1:n.*791C>G
ENST00000678371.1:n.1818C>G
ENST00000678404.1:c.1368C>G	ENSP00000503944.1:p.Asp456Glu
ENST00000678419.1:c.1368C>G	ENSP00000504085.1:p.Asp456Glu
ENST00000678433.1:n.1724C>G
ENST00000678467.1:c.1368C>G	ENSP00000504072.1:p.Asp456Glu
ENST00000678569.1:c.*353C>G	ENSP00000504261.1:n.*353C>G
ENST00000678961.1:n.1723C>G
ENST00000679002.1:n.1547C>G
ENST00000679012.1:c.924C>G	ENSP00000504446.1:p.Asp308Glu
ENST00000679070.1:c.*787C>G	ENSP00000503759.1:n.*787C>G
ENST00000679130.1:c.1368C>G	ENSP00000504845.1:p.Asp456Glu
ENST00000679315.1:c.*1198C>G	ENSP00000503065.1:n.*1198C>G
ENST00000243583.10:c.1245C>G	ENSP00000243583.5:p.Asp415Glu
ENST00000324464.7:c.1368C>G	ENSP00000315118.3:p.Asp456Glu
ENST00000593724.1:n.1483C>G
NM_001142555.2:c.1245C>G	NP_001136027.1:p.Asp415Glu
NM_024876.3:c.1368C>G	NP_079152.3:p.Asp456Glu
XM_005259270.3:c.1530C>G	XP_005259327.2:p.Asp510Glu
XM_005259271.3:c.1368C>G	XP_005259328.1:p.Asp456Glu
XM_005259272.3:c.1368C>G	XP_005259329.1:p.Asp456Glu
XM_005259273.3:c.1368C>G	XP_005259330.1:p.Asp456Glu
XM_006723392.2:c.1368C>G	XP_006723455.1:p.Asp456Glu
XM_006723393.2:c.1368C>G	XP_006723456.1:p.Asp456Glu
XM_011527334.1:c.1368C>G	XP_011525636.1:p.Asp456Glu
XM_011527335.1:c.1227C>G	XP_011525637.1:p.Asp409Glu
XM_011527336.1:c.1398C>G	XP_011525638.1:p.Asp466Glu
XM_011527337.1:c.1368C>G	XP_011525639.1:p.Asp456Glu
XM_011527338.1:c.1368C>G	XP_011525640.1:p.Asp456Glu
NM_024876.4:c.1368C>G MANE Select	NP_079152.3:p.Asp456Glu
NM_001142555.3:c.1245C>G	NP_001136027.1:p.Asp415Glu