Canonical Allele Identifier: CA2406835163

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623792C= , CM000684.2:g.42623792C=	GRCh38
NC_000022.10:g.43019798C= , CM000684.1:g.43019798C=	GRCh37
NC_000022.9:g.41349742C=	NCBI36
NG_012194.1:g.30608G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.862G=	ENSP00000354468.5:p.Glu288=
ENST00000402438.6:c.661G=	ENSP00000385679.1:p.Glu221=
ENST00000407332.6:c.748G=	ENSP00000384457.2:p.Glu250=
ENST00000407623.8:c.661G=	ENSP00000384834.3:p.Glu221=
ENST00000617178.5:c.267G=
ENST00000684963.1:n.2470G=
ENST00000685184.1:n.322G=
ENST00000686523.1:c.*679G=	ENSP00000508940.1:n.*679G=
ENST00000687183.1:n.1006G=
ENST00000687198.1:c.661G=	ENSP00000508492.1:p.Glu221=
ENST00000688117.1:c.829G=	ENSP00000509015.1:p.Glu277=
ENST00000688244.1:c.430G=	ENSP00000510355.1:p.Glu144=
ENST00000689001.1:n.1352G=
ENST00000689195.1:c.646G=	ENSP00000509895.1:p.Glu216=
ENST00000689239.1:n.897G=
ENST00000689795.1:n.991G=
ENST00000690835.1:c.*109G=	ENSP00000509038.1:n.*109G=
ENST00000690993.1:n.1485G=
ENST00000691295.1:c.*213G=	ENSP00000508706.1:n.*213G=
ENST00000691918.1:c.1020G=	ENSP00000509525.1:n.1020G=
ENST00000692152.1:c.661G=	ENSP00000509317.1:p.Glu221=
ENST00000692344.1:n.1217G=
ENST00000693363.1:c.772G=	ENSP00000510411.1:p.Glu258=
ENST00000693367.1:c.730G=	ENSP00000508815.1:p.Glu244=
ENST00000693639.1:c.723G=	ENSP00000510223.1:n.723G=
ENST00000693646.1:c.636G=	ENSP00000508449.1:n.636G=
ENST00000352397.10:c.730G= MANE Select	ENSP00000338461.6:p.Glu244=
ENST00000352397.9:c.730G=	ENSP00000338461.6:p.Glu244=
ENST00000361740.8:c.829G=	ENSP00000354468.4:p.Glu277=
ENST00000402438.5:c.661G=	ENSP00000385679.1:p.Glu221=
ENST00000407332.5:c.661G=	ENSP00000384457.1:p.Glu221=
ENST00000407623.7:c.661G=	ENSP00000384834.3:p.Glu221=
ENST00000470741.1:n.2864G=
NM_000398.6:c.730G=	NP_000389.1:p.Glu244=
NM_001129819.2:c.661G=	NP_001123291.1:p.Glu221=
NM_001171660.1:c.829G=	NP_001165131.1:p.Glu277=
NM_001171661.1:c.661G=	NP_001165132.1:p.Glu221=
NM_007326.4:c.661G=	NP_015565.1:p.Glu221=
NM_000398.7:c.730G= MANE Select	NP_000389.1:p.Glu244=
NM_001171660.2:c.829G=	NP_001165131.1:p.Glu277=