Canonical Allele Identifier: CA2406835170

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623803T= , CM000684.2:g.42623803T=	GRCh38
NC_000022.10:g.43019809T= , CM000684.1:g.43019809T=	GRCh37
NC_000022.9:g.41349753T=	NCBI36
NG_012194.1:g.30597A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.851A=	ENSP00000354468.5:p.Asp284=
ENST00000402438.6:c.650A=	ENSP00000385679.1:p.Asp217=
ENST00000407332.6:c.737A=	ENSP00000384457.2:p.Asp246=
ENST00000407623.8:c.650A=	ENSP00000384834.3:p.Asp217=
ENST00000617178.5:c.256A=
ENST00000684963.1:n.2459A=
ENST00000685184.1:n.311A=
ENST00000686523.1:c.*668A=	ENSP00000508940.1:n.*668A=
ENST00000687183.1:n.995A=
ENST00000687198.1:c.650A=	ENSP00000508492.1:p.Asp217=
ENST00000688117.1:c.818A=	ENSP00000509015.1:p.Asp273=
ENST00000688244.1:c.419A=	ENSP00000510355.1:p.Asp140=
ENST00000689001.1:n.1341A=
ENST00000689195.1:c.635A=	ENSP00000509895.1:p.Asp212=
ENST00000689239.1:n.886A=
ENST00000689795.1:n.980A=
ENST00000690835.1:c.*98A=	ENSP00000509038.1:n.*98A=
ENST00000690993.1:n.1474A=
ENST00000691295.1:c.*202A=	ENSP00000508706.1:n.*202A=
ENST00000691918.1:c.1009A=	ENSP00000509525.1:n.1009A=
ENST00000692152.1:c.650A=	ENSP00000509317.1:p.Asp217=
ENST00000692344.1:n.1206A=
ENST00000693363.1:c.761A=	ENSP00000510411.1:p.Asp254=
ENST00000693367.1:c.719A=	ENSP00000508815.1:p.Asp240=
ENST00000693639.1:c.712A=	ENSP00000510223.1:n.712A=
ENST00000693646.1:c.625A=	ENSP00000508449.1:n.625A=
ENST00000352397.10:c.719A= MANE Select	ENSP00000338461.6:p.Asp240=
ENST00000352397.9:c.719A=	ENSP00000338461.6:p.Asp240=
ENST00000361740.8:c.818A=	ENSP00000354468.4:p.Asp273=
ENST00000402438.5:c.650A=	ENSP00000385679.1:p.Asp217=
ENST00000407332.5:c.650A=	ENSP00000384457.1:p.Asp217=
ENST00000407623.7:c.650A=	ENSP00000384834.3:p.Asp217=
ENST00000470741.1:n.2853A=
NM_000398.6:c.719A=	NP_000389.1:p.Asp240=
NM_001129819.2:c.650A=	NP_001123291.1:p.Asp217=
NM_001171660.1:c.818A=	NP_001165131.1:p.Asp273=
NM_001171661.1:c.650A=	NP_001165132.1:p.Asp217=
NM_007326.4:c.650A=	NP_015565.1:p.Asp217=
NM_000398.7:c.719A= MANE Select	NP_000389.1:p.Asp240=
NM_001171660.2:c.818A=	NP_001165131.1:p.Asp273=