Canonical Allele Identifier: CA2406835194

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623846T= , CM000684.2:g.42623846T=	GRCh38
NC_000022.10:g.43019852T= , CM000684.1:g.43019852T=	GRCh37
NC_000022.9:g.41349796T=	NCBI36
NG_012194.1:g.30554A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.808A=	ENSP00000354468.5:p.Arg270=
ENST00000402438.6:c.607A=	ENSP00000385679.1:p.Arg203=
ENST00000407332.6:c.694A=	ENSP00000384457.2:p.Arg232=
ENST00000407623.8:c.607A=	ENSP00000384834.3:p.Arg203=
ENST00000617178.5:c.213A=
ENST00000684963.1:n.2416A=
ENST00000685184.1:n.268A=
ENST00000686523.1:c.*625A=	ENSP00000508940.1:n.*625A=
ENST00000687183.1:n.952A=
ENST00000687198.1:c.607A=	ENSP00000508492.1:p.Arg203=
ENST00000688117.1:c.775A=	ENSP00000509015.1:p.Arg259=
ENST00000688244.1:c.376A=	ENSP00000510355.1:p.Arg126=
ENST00000689001.1:n.1298A=
ENST00000689195.1:c.592A=	ENSP00000509895.1:p.Arg198=
ENST00000689239.1:n.843A=
ENST00000689795.1:n.937A=
ENST00000690835.1:c.*55A=	ENSP00000509038.1:n.*55A=
ENST00000690993.1:n.1431A=
ENST00000691295.1:c.*159A=	ENSP00000508706.1:n.*159A=
ENST00000691918.1:c.966A=	ENSP00000509525.1:n.966A=
ENST00000692152.1:c.607A=	ENSP00000509317.1:p.Arg203=
ENST00000692344.1:n.1163A=
ENST00000693363.1:c.718A=	ENSP00000510411.1:p.Arg240=
ENST00000693367.1:c.676A=	ENSP00000508815.1:p.Arg226=
ENST00000693639.1:c.669A=	ENSP00000510223.1:n.669A=
ENST00000693646.1:c.582A=	ENSP00000508449.1:n.582A=
ENST00000352397.10:c.676A= MANE Select	ENSP00000338461.6:p.Arg226=
ENST00000352397.9:c.676A=	ENSP00000338461.6:p.Arg226=
ENST00000361740.8:c.775A=	ENSP00000354468.4:p.Arg259=
ENST00000402438.5:c.607A=	ENSP00000385679.1:p.Arg203=
ENST00000407332.5:c.607A=	ENSP00000384457.1:p.Arg203=
ENST00000407623.7:c.607A=	ENSP00000384834.3:p.Arg203=
ENST00000470741.1:n.2810A=
NM_000398.6:c.676A=	NP_000389.1:p.Arg226=
NM_001129819.2:c.607A=	NP_001123291.1:p.Arg203=
NM_001171660.1:c.775A=	NP_001165131.1:p.Arg259=
NM_001171661.1:c.607A=	NP_001165132.1:p.Arg203=
NM_007326.4:c.607A=	NP_015565.1:p.Arg203=
NM_000398.7:c.676A= MANE Select	NP_000389.1:p.Arg226=
NM_001171660.2:c.775A=	NP_001165131.1:p.Arg259=