Canonical Allele Identifier: CA2406835206

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623886G= , CM000684.2:g.42623886G=	GRCh38
NC_000022.10:g.43019892G= , CM000684.1:g.43019892G=	GRCh37
NC_000022.9:g.41349836G=	NCBI36
NG_012194.1:g.30514C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.768C=	ENSP00000354468.5:p.Thr256=
ENST00000402438.6:c.567C=	ENSP00000385679.1:p.Thr189=
ENST00000407332.6:c.654C=	ENSP00000384457.2:p.Thr218=
ENST00000407623.8:c.567C=	ENSP00000384834.3:p.Thr189=
ENST00000617178.5:c.173C=
ENST00000684963.1:n.2376C=
ENST00000685184.1:n.228C=
ENST00000686523.1:c.*585C=	ENSP00000508940.1:n.*585C=
ENST00000687183.1:n.912C=
ENST00000687198.1:c.567C=	ENSP00000508492.1:p.Thr189=
ENST00000688117.1:c.735C=	ENSP00000509015.1:p.Thr245=
ENST00000688244.1:c.336C=	ENSP00000510355.1:p.Thr112=
ENST00000689001.1:n.1258C=
ENST00000689195.1:c.552C=	ENSP00000509895.1:p.Thr184=
ENST00000689239.1:n.803C=
ENST00000689795.1:n.897C=
ENST00000690835.1:c.*15C=	ENSP00000509038.1:n.*15C=
ENST00000690993.1:n.1391C=
ENST00000691295.1:c.*119C=	ENSP00000508706.1:n.*119C=
ENST00000691918.1:c.926C=	ENSP00000509525.1:n.926C=
ENST00000692152.1:c.567C=	ENSP00000509317.1:p.Thr189=
ENST00000692344.1:n.1123C=
ENST00000693363.1:c.678C=	ENSP00000510411.1:p.Thr226=
ENST00000693367.1:c.636C=	ENSP00000508815.1:p.Thr212=
ENST00000693639.1:c.629C=	ENSP00000510223.1:n.629C=
ENST00000693646.1:c.542C=	ENSP00000508449.1:n.542C=
ENST00000352397.10:c.636C= MANE Select	ENSP00000338461.6:p.Thr212=
ENST00000352397.9:c.636C=	ENSP00000338461.6:p.Thr212=
ENST00000361740.8:c.735C=	ENSP00000354468.4:p.Thr245=
ENST00000402438.5:c.567C=	ENSP00000385679.1:p.Thr189=
ENST00000407332.5:c.567C=	ENSP00000384457.1:p.Thr189=
ENST00000407623.7:c.567C=	ENSP00000384834.3:p.Thr189=
ENST00000470741.1:n.2770C=
NM_000398.6:c.636C=	NP_000389.1:p.Thr212=
NM_001129819.2:c.567C=	NP_001123291.1:p.Thr189=
NM_001171660.1:c.735C=	NP_001165131.1:p.Thr245=
NM_001171661.1:c.567C=	NP_001165132.1:p.Thr189=
NM_007326.4:c.567C=	NP_015565.1:p.Thr189=
NM_000398.7:c.636C= MANE Select	NP_000389.1:p.Thr212=
NM_001171660.2:c.735C=	NP_001165131.1:p.Thr245=