Canonical Allele Identifier: CA552793071

Gene: COQ2

Linked Data

• dbSNP Id: rs1359533875
• gnomAD v2: 4-84199967-C-A
• gnomAD v3: 4-83278814-C-A
• gnomAD v4: 4-83278814-C-A
• MyVariant Identifiers: chr4:g.84199967C>A (hg19) ; chr4:g.83278814C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.83278814C>A , CM000666.2:g.83278814C>A	GRCh38
NC_000004.11:g.84199967C>A , CM000666.1:g.84199967C>A	GRCh37
NC_000004.10:g.84418991C>A	NCBI36
NG_015825.1:g.11101G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311469.9:c.570+134G>T	ENSP00000310873.4:n.570+134G>T
ENST00000647002.2:c.420+134G>T MANE Select	ENSP00000495761.2:n.420+134G>T
ENST00000311461.7:c.420+134G>T	ENSP00000311835.7:n.420+134G>T
ENST00000311469.8:c.570+134G>T	ENSP00000310873.4:n.570+134G>T
ENST00000503391.5:c.420+134G>T	ENSP00000426242.1:n.420+134G>T
ENST00000503915.5:c.111+134G>T	ENSP00000427146.1:n.111+134G>T
ENST00000514935.1:n.332+134G>T
NM_015697.7:c.570+134G>T	NP_056512.5:n.570+134G>T
XM_011531855.1:c.570+134G>T	XP_011530157.1:n.570+134G>T
XM_011531856.1:c.570+134G>T	XP_011530158.1:n.570+134G>T
XM_011531857.1:c.570+134G>T	XP_011530159.1:n.570+134G>T
XM_011531858.1:c.570+134G>T	XP_011530160.1:n.570+134G>T
XM_011531859.1:c.570+134G>T	XP_011530161.1:n.570+134G>T
XM_011531860.1:c.570+134G>T	XP_011530162.1:n.570+134G>T
XM_011531861.1:c.570+134G>T	XP_011530163.1:n.570+134G>T
XM_011531862.1:c.570+134G>T	XP_011530164.1:n.570+134G>T
XM_011531863.1:c.570+134G>T	XP_011530165.1:n.570+134G>T
XM_011531864.1:c.570+134G>T	XP_011530166.1:n.570+134G>T
XM_011531865.1:c.570+134G>T	XP_011530167.1:n.570+134G>T
XM_011531866.1:c.570+134G>T	XP_011530168.1:n.570+134G>T
XM_011531867.1:c.216+134G>T	XP_011530169.1:n.216+134G>T
XR_427543.2:n.729+134G>T
XR_938721.1:n.745+134G>T
NM_001358921.1:c.420+134G>T	NP_001345850.1:n.420+134G>T
NM_015697.8:c.570+134G>T	NP_056512.5:n.570+134G>T
XM_011531855.3:c.420+134G>T	XP_011530157.2:n.420+134G>T
XM_011531857.3:c.420+134G>T	XP_011530159.2:n.420+134G>T
XM_011531859.3:c.420+134G>T	XP_011530161.2:n.420+134G>T
XM_011531860.3:c.420+134G>T	XP_011530162.2:n.420+134G>T
XM_011531862.3:c.420+134G>T	XP_011530164.2:n.420+134G>T
XM_011531863.3:c.420+134G>T	XP_011530165.2:n.420+134G>T
XM_011531866.3:c.420+134G>T	XP_011530168.2:n.420+134G>T
XM_011531867.3:c.216+134G>T	XP_011530169.1:n.216+134G>T
XM_017008031.2:c.216+134G>T	XP_016863520.1:n.216+134G>T
XR_001741203.2:n.451+134G>T
XR_001741204.2:n.451+134G>T
XR_427543.4:n.451+134G>T
XR_938721.3:n.451+134G>T
NM_001358921.2:c.420+134G>T MANE Select	NP_001345850.1:n.420+134G>T
NM_015697.9:c.570+134G>T	NP_056512.5:n.570+134G>T