Canonical Allele Identifier: CA2406835256

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623970A= , CM000684.2:g.42623970A=	GRCh38
NC_000022.10:g.43019976A= , CM000684.1:g.43019976A=	GRCh37
NC_000022.9:g.41349920A=	NCBI36
NG_012194.1:g.30430T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.766-82T=	ENSP00000354468.5:n.766-82T=
ENST00000402438.6:c.565-82T=	ENSP00000385679.1:n.565-82T=
ENST00000407332.6:c.652-82T=	ENSP00000384457.2:n.652-82T=
ENST00000407623.8:c.565-82T=	ENSP00000384834.3:n.565-82T=
ENST00000617178.5:c.171-82T=
ENST00000684963.1:n.2374-82T=
ENST00000685184.1:n.144T=
ENST00000686523.1:c.*583-82T=	ENSP00000508940.1:n.*583-82T=
ENST00000687183.1:n.910-82T=
ENST00000687198.1:c.565-82T=	ENSP00000508492.1:n.565-82T=
ENST00000688117.1:c.733-82T=	ENSP00000509015.1:n.733-82T=
ENST00000688244.1:c.334-82T=	ENSP00000510355.1:n.334-82T=
ENST00000689001.1:n.1256-82T=
ENST00000689195.1:c.550-82T=	ENSP00000509895.1:n.550-82T=
ENST00000689239.1:n.801-82T=
ENST00000689795.1:n.895-82T=
ENST00000690835.1:c.*13-82T=	ENSP00000509038.1:n.*13-82T=
ENST00000690993.1:n.1389-82T=
ENST00000691295.1:c.*117-82T=	ENSP00000508706.1:n.*117-82T=
ENST00000691918.1:c.924-82T=	ENSP00000509525.1:n.924-82T=
ENST00000692152.1:c.565-82T=	ENSP00000509317.1:n.565-82T=
ENST00000692344.1:n.1121-82T=
ENST00000693363.1:c.676-82T=	ENSP00000510411.1:n.676-82T=
ENST00000693367.1:c.634-82T=	ENSP00000508815.1:n.634-82T=
ENST00000693639.1:c.627-82T=	ENSP00000510223.1:n.627-82T=
ENST00000693646.1:c.540-82T=	ENSP00000508449.1:n.540-82T=
ENST00000352397.10:c.634-82T= MANE Select	ENSP00000338461.6:n.634-82T=
ENST00000352397.9:c.634-82T=	ENSP00000338461.6:n.634-82T=
ENST00000361740.8:c.733-82T=	ENSP00000354468.4:n.733-82T=
ENST00000402438.5:c.565-82T=	ENSP00000385679.1:n.565-82T=
ENST00000407332.5:c.565-82T=	ENSP00000384457.1:n.565-82T=
ENST00000407623.7:c.565-82T=	ENSP00000384834.3:n.565-82T=
ENST00000470741.1:n.2768-82T=
NM_000398.6:c.634-82T=	NP_000389.1:n.634-82T=
NM_001129819.2:c.565-82T=	NP_001123291.1:n.565-82T=
NM_001171660.1:c.733-82T=	NP_001165131.1:n.733-82T=
NM_001171661.1:c.565-82T=	NP_001165132.1:n.565-82T=
NM_007326.4:c.565-82T=	NP_015565.1:n.565-82T=
NM_000398.7:c.634-82T= MANE Select	NP_000389.1:n.634-82T=
NM_001171660.2:c.733-82T=	NP_001165131.1:n.733-82T=