Canonical Allele Identifier: CA405960826

Gene: COQ8B

Linked Data

• MyVariant Identifiers: chr19:g.41206271C>A (hg19) ; chr19:g.40700366C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40700366C>A , CM000681.2:g.40700366C>A	GRCh38
NC_000019.9:g.41206271C>A , CM000681.1:g.41206271C>A	GRCh37
NC_000019.8:g.45898111C>A	NCBI36
NG_027800.1:g.21520G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.979G>T MANE Select	ENSP00000315118.3:p.Ala327Ser
ENST00000593724.2:n.2802G>T
ENST00000594490.6:c.901G>T	ENSP00000471310.2:p.Ala301Ser
ENST00000594720.6:c.979G>T	ENSP00000470876.2:p.Ala327Ser
ENST00000596455.6:n.1271G>T
ENST00000601967.6:c.979G>T	ENSP00000470916.2:p.Ala327Ser
ENST00000676555.1:c.979G>T	ENSP00000503387.1:p.Ala327Ser
ENST00000676578.1:c.*721G>T	ENSP00000504076.1:n.*721G>T
ENST00000676960.1:n.1104G>T
ENST00000676962.1:n.1258G>T
ENST00000677018.1:c.979G>T	ENSP00000503480.1:p.Ala327Ser
ENST00000677039.1:n.3182G>T
ENST00000677399.1:n.1421G>T
ENST00000677496.1:c.652G>T	ENSP00000504773.1:p.Ala218Ser
ENST00000677517.1:c.652G>T	ENSP00000503519.1:p.Ala218Ser
ENST00000677633.1:c.*402G>T	ENSP00000503645.1:n.*402G>T
ENST00000677800.1:c.*4083G>T	ENSP00000503794.1:n.*4083G>T
ENST00000678057.1:c.*543G>T	ENSP00000503762.1:n.*543G>T
ENST00000678119.1:n.1173G>T
ENST00000678166.1:n.1122G>T
ENST00000678312.1:n.1316G>T
ENST00000678316.1:c.*402G>T	ENSP00000504112.1:n.*402G>T
ENST00000678371.1:n.1429G>T
ENST00000678404.1:c.979G>T	ENSP00000503944.1:p.Ala327Ser
ENST00000678419.1:c.979G>T	ENSP00000504085.1:p.Ala327Ser
ENST00000678433.1:n.1335G>T
ENST00000678467.1:c.979G>T	ENSP00000504072.1:p.Ala327Ser
ENST00000678569.1:c.975G>T	ENSP00000504261.1:p.Trp325Cys
ENST00000678961.1:n.1334G>T
ENST00000679002.1:n.1158G>T
ENST00000679012.1:c.535G>T	ENSP00000504446.1:p.Ala179Ser
ENST00000679070.1:c.*398G>T	ENSP00000503759.1:n.*398G>T
ENST00000679130.1:c.979G>T	ENSP00000504845.1:p.Ala327Ser
ENST00000679315.1:c.*809G>T	ENSP00000503065.1:n.*809G>T
ENST00000243583.10:c.856G>T	ENSP00000243583.5:p.Ala286Ser
ENST00000324464.7:c.979G>T	ENSP00000315118.3:p.Ala327Ser
ENST00000593724.1:n.1094G>T
NM_001142555.2:c.856G>T	NP_001136027.1:p.Ala286Ser
NM_024876.3:c.979G>T	NP_079152.3:p.Ala327Ser
XM_005259270.3:c.1141G>T	XP_005259327.2:p.Ala381Ser
XM_005259271.3:c.979G>T	XP_005259328.1:p.Ala327Ser
XM_005259272.3:c.979G>T	XP_005259329.1:p.Ala327Ser
XM_005259273.3:c.979G>T	XP_005259330.1:p.Ala327Ser
XM_006723392.2:c.979G>T	XP_006723455.1:p.Ala327Ser
XM_006723393.2:c.979G>T	XP_006723456.1:p.Ala327Ser
XM_011527334.1:c.979G>T	XP_011525636.1:p.Ala327Ser
XM_011527335.1:c.838G>T	XP_011525637.1:p.Ala280Ser
XM_011527336.1:c.1009G>T	XP_011525638.1:p.Ala337Ser
XM_011527337.1:c.979G>T	XP_011525639.1:p.Ala327Ser
XM_011527338.1:c.979G>T	XP_011525640.1:p.Ala327Ser
NM_024876.4:c.979G>T MANE Select	NP_079152.3:p.Ala327Ser
NM_001142555.3:c.856G>T	NP_001136027.1:p.Ala286Ser