Canonical Allele Identifier: CA507686442

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41198264G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40692359G>C , CM000681.2:g.40692359G>C	GRCh38
NC_000019.9:g.41198264G>C , CM000681.1:g.41198264G>C	GRCh37
NC_000019.8:g.45890104G>C	NCBI36
NG_027800.1:g.29527C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.1311C>G MANE Select	ENSP00000315118.3:p.Ala437=
ENST00000593724.2:n.3134C>G
ENST00000594490.6:c.1233C>G	ENSP00000471310.2:p.Ala411=
ENST00000594720.6:c.1311C>G	ENSP00000470876.2:p.Ala437=
ENST00000596455.6:n.1603C>G
ENST00000601967.6:c.1311C>G	ENSP00000470916.2:p.Ala437=
ENST00000676555.1:c.*736C>G	ENSP00000503387.1:n.*736C>G
ENST00000676578.1:c.*1053C>G	ENSP00000504076.1:n.*1053C>G
ENST00000676960.1:n.1436C>G
ENST00000676962.1:n.1590C>G
ENST00000677018.1:c.1311C>G	ENSP00000503480.1:p.Ala437=
ENST00000677039.1:n.3514C>G
ENST00000677399.1:n.1753C>G
ENST00000677496.1:c.984C>G	ENSP00000504773.1:p.Ala328=
ENST00000677517.1:c.984C>G	ENSP00000503519.1:p.Ala328=
ENST00000677633.1:c.*734C>G	ENSP00000503645.1:n.*734C>G
ENST00000677800.1:c.*4415C>G	ENSP00000503794.1:n.*4415C>G
ENST00000678057.1:c.*875C>G	ENSP00000503762.1:n.*875C>G
ENST00000678119.1:n.1505C>G
ENST00000678166.1:n.1454C>G
ENST00000678312.1:n.1648C>G
ENST00000678316.1:c.*734C>G	ENSP00000504112.1:n.*734C>G
ENST00000678371.1:n.1761C>G
ENST00000678404.1:c.1311C>G	ENSP00000503944.1:p.Ala437=
ENST00000678419.1:c.1311C>G	ENSP00000504085.1:p.Ala437=
ENST00000678433.1:n.1667C>G
ENST00000678467.1:c.1311C>G	ENSP00000504072.1:p.Ala437=
ENST00000678569.1:c.*296C>G	ENSP00000504261.1:n.*296C>G
ENST00000678961.1:n.1666C>G
ENST00000679002.1:n.1490C>G
ENST00000679012.1:c.867C>G	ENSP00000504446.1:p.Ala289=
ENST00000679070.1:c.*730C>G	ENSP00000503759.1:n.*730C>G
ENST00000679130.1:c.1311C>G	ENSP00000504845.1:p.Ala437=
ENST00000679315.1:c.*1141C>G	ENSP00000503065.1:n.*1141C>G
ENST00000243583.10:c.1188C>G	ENSP00000243583.5:p.Ala396=
ENST00000324464.7:c.1311C>G	ENSP00000315118.3:p.Ala437=
ENST00000593724.1:n.1426C>G
NM_001142555.2:c.1188C>G	NP_001136027.1:p.Ala396=
NM_024876.3:c.1311C>G	NP_079152.3:p.Ala437=
XM_005259270.3:c.1473C>G	XP_005259327.2:p.Ala491=
XM_005259271.3:c.1311C>G	XP_005259328.1:p.Ala437=
XM_005259272.3:c.1311C>G	XP_005259329.1:p.Ala437=
XM_005259273.3:c.1311C>G	XP_005259330.1:p.Ala437=
XM_006723392.2:c.1311C>G	XP_006723455.1:p.Ala437=
XM_006723393.2:c.1311C>G	XP_006723456.1:p.Ala437=
XM_011527334.1:c.1311C>G	XP_011525636.1:p.Ala437=
XM_011527335.1:c.1170C>G	XP_011525637.1:p.Ala390=
XM_011527336.1:c.1341C>G	XP_011525638.1:p.Ala447=
XM_011527337.1:c.1311C>G	XP_011525639.1:p.Ala437=
XM_011527338.1:c.1311C>G	XP_011525640.1:p.Ala437=
NM_024876.4:c.1311C>G MANE Select	NP_079152.3:p.Ala437=
NM_001142555.3:c.1188C>G	NP_001136027.1:p.Ala396=