Canonical Allele Identifier: CA507504035

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41209641C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40703736C>A , CM000681.2:g.40703736C>A	GRCh38
NC_000019.9:g.41209641C>A , CM000681.1:g.41209641C>A	GRCh37
NC_000019.8:g.45901481C>A	NCBI36
NG_027800.1:g.18150G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.696G>T MANE Select	ENSP00000315118.3:p.Thr232=
ENST00000593724.2:n.393-114G>T
ENST00000594490.6:c.618G>T	ENSP00000471310.2:p.Thr206=
ENST00000594720.6:c.696G>T	ENSP00000470876.2:p.Thr232=
ENST00000596455.6:n.988G>T
ENST00000601967.6:c.696G>T	ENSP00000470916.2:p.Thr232=
ENST00000676555.1:c.696G>T	ENSP00000503387.1:p.Thr232=
ENST00000676578.1:c.*438G>T	ENSP00000504076.1:n.*438G>T
ENST00000676960.1:n.821G>T
ENST00000676962.1:n.975G>T
ENST00000677018.1:c.696G>T	ENSP00000503480.1:p.Thr232=
ENST00000677039.1:n.751G>T
ENST00000677399.1:n.1138G>T
ENST00000677496.1:c.369G>T	ENSP00000504773.1:p.Thr123=
ENST00000677517.1:c.369G>T	ENSP00000503519.1:p.Thr123=
ENST00000677633.1:c.*119G>T	ENSP00000503645.1:n.*119G>T
ENST00000677800.1:c.*3800G>T	ENSP00000503794.1:n.*3800G>T
ENST00000678057.1:c.*260G>T	ENSP00000503762.1:n.*260G>T
ENST00000678119.1:n.890G>T
ENST00000678166.1:n.861-114G>T
ENST00000678312.1:n.1033G>T
ENST00000678316.1:c.*119G>T	ENSP00000504112.1:n.*119G>T
ENST00000678371.1:n.1054G>T
ENST00000678404.1:c.696G>T	ENSP00000503944.1:p.Thr232=
ENST00000678419.1:c.696G>T	ENSP00000504085.1:p.Thr232=
ENST00000678433.1:n.1056G>T
ENST00000678467.1:c.696G>T	ENSP00000504072.1:p.Thr232=
ENST00000678569.1:c.696G>T	ENSP00000504261.1:p.Thr232=
ENST00000678961.1:n.879G>T
ENST00000679002.1:n.875G>T
ENST00000679012.1:c.252G>T	ENSP00000504446.1:p.Thr84=
ENST00000679070.1:c.*119G>T	ENSP00000503759.1:n.*119G>T
ENST00000679130.1:c.696G>T	ENSP00000504845.1:p.Thr232=
ENST00000679315.1:c.*526G>T	ENSP00000503065.1:n.*526G>T
ENST00000243583.10:c.573G>T	ENSP00000243583.5:p.Thr191=
ENST00000324464.7:c.696G>T	ENSP00000315118.3:p.Thr232=
ENST00000595254.5:c.369G>T	ENSP00000470894.1:p.Thr123=
ENST00000596455.5:n.816G>T
ENST00000599643.5:c.336-114G>T	ENSP00000471192.1:n.336-114G>T
ENST00000601304.5:c.*470G>T	ENSP00000472519.1:n.*470G>T
NM_001142555.2:c.573G>T	NP_001136027.1:p.Thr191=
NM_024876.3:c.696G>T	NP_079152.3:p.Thr232=
XM_005259270.3:c.858G>T	XP_005259327.2:p.Thr286=
XM_005259271.3:c.696G>T	XP_005259328.1:p.Thr232=
XM_005259272.3:c.696G>T	XP_005259329.1:p.Thr232=
XM_005259273.3:c.696G>T	XP_005259330.1:p.Thr232=
XM_006723392.2:c.696G>T	XP_006723455.1:p.Thr232=
XM_006723393.2:c.696G>T	XP_006723456.1:p.Thr232=
XM_011527334.1:c.696G>T	XP_011525636.1:p.Thr232=
XM_011527335.1:c.577-114G>T	XP_011525637.1:n.577-114G>T
XM_011527336.1:c.726G>T	XP_011525638.1:p.Thr242=
XM_011527337.1:c.696G>T	XP_011525639.1:p.Thr232=
XM_011527338.1:c.696G>T	XP_011525640.1:p.Thr232=
NM_024876.4:c.696G>T MANE Select	NP_079152.3:p.Thr232=
NM_001142555.3:c.573G>T	NP_001136027.1:p.Thr191=