Canonical Allele Identifier: CA2406835168

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623800C= , CM000684.2:g.42623800C=	GRCh38
NC_000022.10:g.43019806C= , CM000684.1:g.43019806C=	GRCh37
NC_000022.9:g.41349750C=	NCBI36
NG_012194.1:g.30600G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.854G=	ENSP00000354468.5:p.Arg285=
ENST00000402438.6:c.653G=	ENSP00000385679.1:p.Arg218=
ENST00000407332.6:c.740G=	ENSP00000384457.2:p.Arg247=
ENST00000407623.8:c.653G=	ENSP00000384834.3:p.Arg218=
ENST00000617178.5:c.259G=
ENST00000684963.1:n.2462G=
ENST00000685184.1:n.314G=
ENST00000686523.1:c.*671G=	ENSP00000508940.1:n.*671G=
ENST00000687183.1:n.998G=
ENST00000687198.1:c.653G=	ENSP00000508492.1:p.Arg218=
ENST00000688117.1:c.821G=	ENSP00000509015.1:p.Arg274=
ENST00000688244.1:c.422G=	ENSP00000510355.1:p.Arg141=
ENST00000689001.1:n.1344G=
ENST00000689195.1:c.638G=	ENSP00000509895.1:p.Arg213=
ENST00000689239.1:n.889G=
ENST00000689795.1:n.983G=
ENST00000690835.1:c.*101G=	ENSP00000509038.1:n.*101G=
ENST00000690993.1:n.1477G=
ENST00000691295.1:c.*205G=	ENSP00000508706.1:n.*205G=
ENST00000691918.1:c.1012G=	ENSP00000509525.1:n.1012G=
ENST00000692152.1:c.653G=	ENSP00000509317.1:p.Arg218=
ENST00000692344.1:n.1209G=
ENST00000693363.1:c.764G=	ENSP00000510411.1:p.Arg255=
ENST00000693367.1:c.722G=	ENSP00000508815.1:p.Arg241=
ENST00000693639.1:c.715G=	ENSP00000510223.1:n.715G=
ENST00000693646.1:c.628G=	ENSP00000508449.1:n.628G=
ENST00000352397.10:c.722G= MANE Select	ENSP00000338461.6:p.Arg241=
ENST00000352397.9:c.722G=	ENSP00000338461.6:p.Arg241=
ENST00000361740.8:c.821G=	ENSP00000354468.4:p.Arg274=
ENST00000402438.5:c.653G=	ENSP00000385679.1:p.Arg218=
ENST00000407332.5:c.653G=	ENSP00000384457.1:p.Arg218=
ENST00000407623.7:c.653G=	ENSP00000384834.3:p.Arg218=
ENST00000470741.1:n.2856G=
NM_000398.6:c.722G=	NP_000389.1:p.Arg241=
NM_001129819.2:c.653G=	NP_001123291.1:p.Arg218=
NM_001171660.1:c.821G=	NP_001165131.1:p.Arg274=
NM_001171661.1:c.653G=	NP_001165132.1:p.Arg218=
NM_007326.4:c.653G=	NP_015565.1:p.Arg218=
NM_000398.7:c.722G= MANE Select	NP_000389.1:p.Arg241=
NM_001171660.2:c.821G=	NP_001165131.1:p.Arg274=