Canonical Allele Identifier: CA405957943

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41198223G>C (hg19) ; chr19:g.40692318G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40692318G>C , CM000681.2:g.40692318G>C	GRCh38
NC_000019.9:g.41198223G>C , CM000681.1:g.41198223G>C	GRCh37
NC_000019.8:g.45890063G>C	NCBI36
NG_027800.1:g.29568C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.1352C>G MANE Select	ENSP00000315118.3:p.Thr451Ser
ENST00000593724.2:n.3175C>G
ENST00000594490.6:c.1274C>G	ENSP00000471310.2:p.Thr425Ser
ENST00000594720.6:c.1352C>G	ENSP00000470876.2:p.Thr451Ser
ENST00000596455.6:n.1644C>G
ENST00000601967.6:c.1352C>G	ENSP00000470916.2:p.Thr451Ser
ENST00000676555.1:c.*777C>G	ENSP00000503387.1:n.*777C>G
ENST00000676578.1:c.*1094C>G	ENSP00000504076.1:n.*1094C>G
ENST00000676960.1:n.1477C>G
ENST00000676962.1:n.1631C>G
ENST00000677018.1:c.1352C>G	ENSP00000503480.1:p.Thr451Ser
ENST00000677039.1:n.3555C>G
ENST00000677399.1:n.1794C>G
ENST00000677496.1:c.1025C>G	ENSP00000504773.1:p.Thr342Ser
ENST00000677517.1:c.1025C>G	ENSP00000503519.1:p.Thr342Ser
ENST00000677633.1:c.*775C>G	ENSP00000503645.1:n.*775C>G
ENST00000677800.1:c.*4456C>G	ENSP00000503794.1:n.*4456C>G
ENST00000678057.1:c.*916C>G	ENSP00000503762.1:n.*916C>G
ENST00000678119.1:n.1546C>G
ENST00000678166.1:n.1495C>G
ENST00000678312.1:n.1689C>G
ENST00000678316.1:c.*775C>G	ENSP00000504112.1:n.*775C>G
ENST00000678371.1:n.1802C>G
ENST00000678404.1:c.1352C>G	ENSP00000503944.1:p.Thr451Ser
ENST00000678419.1:c.1352C>G	ENSP00000504085.1:p.Thr451Ser
ENST00000678433.1:n.1708C>G
ENST00000678467.1:c.1352C>G	ENSP00000504072.1:p.Thr451Ser
ENST00000678569.1:c.*337C>G	ENSP00000504261.1:n.*337C>G
ENST00000678961.1:n.1707C>G
ENST00000679002.1:n.1531C>G
ENST00000679012.1:c.908C>G	ENSP00000504446.1:p.Thr303Ser
ENST00000679070.1:c.*771C>G	ENSP00000503759.1:n.*771C>G
ENST00000679130.1:c.1352C>G	ENSP00000504845.1:p.Thr451Ser
ENST00000679315.1:c.*1182C>G	ENSP00000503065.1:n.*1182C>G
ENST00000243583.10:c.1229C>G	ENSP00000243583.5:p.Thr410Ser
ENST00000324464.7:c.1352C>G	ENSP00000315118.3:p.Thr451Ser
ENST00000593724.1:n.1467C>G
NM_001142555.2:c.1229C>G	NP_001136027.1:p.Thr410Ser
NM_024876.3:c.1352C>G	NP_079152.3:p.Thr451Ser
XM_005259270.3:c.1514C>G	XP_005259327.2:p.Thr505Ser
XM_005259271.3:c.1352C>G	XP_005259328.1:p.Thr451Ser
XM_005259272.3:c.1352C>G	XP_005259329.1:p.Thr451Ser
XM_005259273.3:c.1352C>G	XP_005259330.1:p.Thr451Ser
XM_006723392.2:c.1352C>G	XP_006723455.1:p.Thr451Ser
XM_006723393.2:c.1352C>G	XP_006723456.1:p.Thr451Ser
XM_011527334.1:c.1352C>G	XP_011525636.1:p.Thr451Ser
XM_011527335.1:c.1211C>G	XP_011525637.1:p.Thr404Ser
XM_011527336.1:c.1382C>G	XP_011525638.1:p.Thr461Ser
XM_011527337.1:c.1352C>G	XP_011525639.1:p.Thr451Ser
XM_011527338.1:c.1352C>G	XP_011525640.1:p.Thr451Ser
NM_024876.4:c.1352C>G MANE Select	NP_079152.3:p.Thr451Ser
NM_001142555.3:c.1229C>G	NP_001136027.1:p.Thr410Ser