Canonical Allele Identifier: CA405958103

Gene: COQ8B

Linked Data

• gnomAD v4: 19-40692358-G-A
• MyVariant Identifiers: chr19:g.41198263G>A (hg19) ; chr19:g.40692358G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40692358G>A , CM000681.2:g.40692358G>A	GRCh38
NC_000019.9:g.41198263G>A , CM000681.1:g.41198263G>A	GRCh37
NC_000019.8:g.45890103G>A	NCBI36
NG_027800.1:g.29528C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324464.8:c.1312C>T MANE Select	ENSP00000315118.3:p.His438Tyr
ENST00000593724.2:n.3135C>T
ENST00000594490.6:c.1234C>T	ENSP00000471310.2:p.His412Tyr
ENST00000594720.6:c.1312C>T	ENSP00000470876.2:p.His438Tyr
ENST00000596455.6:n.1604C>T
ENST00000601967.6:c.1312C>T	ENSP00000470916.2:p.His438Tyr
ENST00000676555.1:c.*737C>T	ENSP00000503387.1:n.*737C>T
ENST00000676578.1:c.*1054C>T	ENSP00000504076.1:n.*1054C>T
ENST00000676960.1:n.1437C>T
ENST00000676962.1:n.1591C>T
ENST00000677018.1:c.1312C>T	ENSP00000503480.1:p.His438Tyr
ENST00000677039.1:n.3515C>T
ENST00000677399.1:n.1754C>T
ENST00000677496.1:c.985C>T	ENSP00000504773.1:p.His329Tyr
ENST00000677517.1:c.985C>T	ENSP00000503519.1:p.His329Tyr
ENST00000677633.1:c.*735C>T	ENSP00000503645.1:n.*735C>T
ENST00000677800.1:c.*4416C>T	ENSP00000503794.1:n.*4416C>T
ENST00000678057.1:c.*876C>T	ENSP00000503762.1:n.*876C>T
ENST00000678119.1:n.1506C>T
ENST00000678166.1:n.1455C>T
ENST00000678312.1:n.1649C>T
ENST00000678316.1:c.*735C>T	ENSP00000504112.1:n.*735C>T
ENST00000678371.1:n.1762C>T
ENST00000678404.1:c.1312C>T	ENSP00000503944.1:p.His438Tyr
ENST00000678419.1:c.1312C>T	ENSP00000504085.1:p.His438Tyr
ENST00000678433.1:n.1668C>T
ENST00000678467.1:c.1312C>T	ENSP00000504072.1:p.His438Tyr
ENST00000678569.1:c.*297C>T	ENSP00000504261.1:n.*297C>T
ENST00000678961.1:n.1667C>T
ENST00000679002.1:n.1491C>T
ENST00000679012.1:c.868C>T	ENSP00000504446.1:p.His290Tyr
ENST00000679070.1:c.*731C>T	ENSP00000503759.1:n.*731C>T
ENST00000679130.1:c.1312C>T	ENSP00000504845.1:p.His438Tyr
ENST00000679315.1:c.*1142C>T	ENSP00000503065.1:n.*1142C>T
ENST00000243583.10:c.1189C>T	ENSP00000243583.5:p.His397Tyr
ENST00000324464.7:c.1312C>T	ENSP00000315118.3:p.His438Tyr
ENST00000593724.1:n.1427C>T
NM_001142555.2:c.1189C>T	NP_001136027.1:p.His397Tyr
NM_024876.3:c.1312C>T	NP_079152.3:p.His438Tyr
XM_005259270.3:c.1474C>T	XP_005259327.2:p.His492Tyr
XM_005259271.3:c.1312C>T	XP_005259328.1:p.His438Tyr
XM_005259272.3:c.1312C>T	XP_005259329.1:p.His438Tyr
XM_005259273.3:c.1312C>T	XP_005259330.1:p.His438Tyr
XM_006723392.2:c.1312C>T	XP_006723455.1:p.His438Tyr
XM_006723393.2:c.1312C>T	XP_006723456.1:p.His438Tyr
XM_011527334.1:c.1312C>T	XP_011525636.1:p.His438Tyr
XM_011527335.1:c.1171C>T	XP_011525637.1:p.His391Tyr
XM_011527336.1:c.1342C>T	XP_011525638.1:p.His448Tyr
XM_011527337.1:c.1312C>T	XP_011525639.1:p.His438Tyr
XM_011527338.1:c.1312C>T	XP_011525640.1:p.His438Tyr
NM_024876.4:c.1312C>T MANE Select	NP_079152.3:p.His438Tyr
NM_001142555.3:c.1189C>T	NP_001136027.1:p.His397Tyr