Canonical Allele Identifier: CA1139848182

Gene: CYB561D1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109499822C= , CM000663.2:g.109499822C=	GRCh38
NC_000001.10:g.110042444C= , CM000663.1:g.110042444C=	GRCh37
NC_000001.9:g.109843967C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420578.7:c.*3563C= MANE Select	ENSP00000413530.2:n.*3563C=
ENST00000310611.8:c.*3955C=	ENSP00000309324.4:n.*3955C=
ENST00000430195.2:c.*4047C=	ENSP00000416898.2:n.*4047C=
ENST00000528785.1:c.687-2561C=	ENSP00000434344.1:n.687-2561C=
NM_001134400.1:c.*3563C=	NP_001127872.1:n.*3563C=
NM_001134402.1:c.*3563C=	NP_001127874.1:n.*3563C=
NM_001134403.1:c.*3955C=	NP_001127875.1:n.*3955C=
NM_001134404.1:c.*4047C=	NP_001127876.1:n.*4047C=
NM_182580.2:c.*3563C=	NP_872386.1:n.*3563C=
XM_005270775.2:c.*3563C=	XP_005270832.1:n.*3563C=
XM_005270776.2:c.*3563C=	XP_005270833.1:n.*3563C=
XM_005270777.2:c.*3563C=	XP_005270834.1:n.*3563C=
XM_011541286.1:c.*3563C=	XP_011539588.1:n.*3563C=
XM_011541287.1:c.*3563C=	XP_011539589.1:n.*3563C=
XM_005270776.3:c.*3563C=	XP_005270833.1:n.*3563C=
XM_011541286.2:c.*3563C=	XP_011539588.1:n.*3563C=
XM_011541287.3:c.*3563C=	XP_011539589.2:n.*3563C=
XM_017001079.1:c.*3563C=	XP_016856568.1:n.*3563C=
NM_001134404.2:c.*4047C=	NP_001127876.1:n.*4047C=
NM_001134400.2:c.*3563C=	NP_001127872.1:n.*3563C=
NM_001134402.2:c.*3563C=	NP_001127874.1:n.*3563C=
NM_001134403.2:c.*3955C=	NP_001127875.1:n.*3955C=
NM_182580.3:c.*3563C= MANE Select	NP_872386.1:n.*3563C=