Canonical Allele Identifier: CA2406835167

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623797G= , CM000684.2:g.42623797G=	GRCh38
NC_000022.10:g.43019803G= , CM000684.1:g.43019803G=	GRCh37
NC_000022.9:g.41349747G=	NCBI36
NG_012194.1:g.30603C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.857C=	ENSP00000354468.5:p.Ala286=
ENST00000402438.6:c.656C=	ENSP00000385679.1:p.Ala219=
ENST00000407332.6:c.743C=	ENSP00000384457.2:p.Ala248=
ENST00000407623.8:c.656C=	ENSP00000384834.3:p.Ala219=
ENST00000617178.5:c.262C=
ENST00000684963.1:n.2465C=
ENST00000685184.1:n.317C=
ENST00000686523.1:c.*674C=	ENSP00000508940.1:n.*674C=
ENST00000687183.1:n.1001C=
ENST00000687198.1:c.656C=	ENSP00000508492.1:p.Ala219=
ENST00000688117.1:c.824C=	ENSP00000509015.1:p.Ala275=
ENST00000688244.1:c.425C=	ENSP00000510355.1:p.Ala142=
ENST00000689001.1:n.1347C=
ENST00000689195.1:c.641C=	ENSP00000509895.1:p.Ala214=
ENST00000689239.1:n.892C=
ENST00000689795.1:n.986C=
ENST00000690835.1:c.*104C=	ENSP00000509038.1:n.*104C=
ENST00000690993.1:n.1480C=
ENST00000691295.1:c.*208C=	ENSP00000508706.1:n.*208C=
ENST00000691918.1:c.1015C=	ENSP00000509525.1:n.1015C=
ENST00000692152.1:c.656C=	ENSP00000509317.1:p.Ala219=
ENST00000692344.1:n.1212C=
ENST00000693363.1:c.767C=	ENSP00000510411.1:p.Ala256=
ENST00000693367.1:c.725C=	ENSP00000508815.1:p.Ala242=
ENST00000693639.1:c.718C=	ENSP00000510223.1:n.718C=
ENST00000693646.1:c.631C=	ENSP00000508449.1:n.631C=
ENST00000352397.10:c.725C= MANE Select	ENSP00000338461.6:p.Ala242=
ENST00000352397.9:c.725C=	ENSP00000338461.6:p.Ala242=
ENST00000361740.8:c.824C=	ENSP00000354468.4:p.Ala275=
ENST00000402438.5:c.656C=	ENSP00000385679.1:p.Ala219=
ENST00000407332.5:c.656C=	ENSP00000384457.1:p.Ala219=
ENST00000407623.7:c.656C=	ENSP00000384834.3:p.Ala219=
ENST00000470741.1:n.2859C=
NM_000398.6:c.725C=	NP_000389.1:p.Ala242=
NM_001129819.2:c.656C=	NP_001123291.1:p.Ala219=
NM_001171660.1:c.824C=	NP_001165131.1:p.Ala275=
NM_001171661.1:c.656C=	NP_001165132.1:p.Ala219=
NM_007326.4:c.656C=	NP_015565.1:p.Ala219=
NM_000398.7:c.725C= MANE Select	NP_000389.1:p.Ala242=
NM_001171660.2:c.824C=	NP_001165131.1:p.Ala275=