Canonical Allele Identifier: CA10269764

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42628183G>A , CM000684.2:g.42628183G>A	GRCh38
NC_000022.10:g.43024189G>A , CM000684.1:g.43024189G>A	GRCh37
NC_000022.9:g.41354133G>A	NCBI36
NG_012194.1:g.26217C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.432C>T	ENSP00000354468.5:p.Gly144=
ENST00000402438.6:c.363C>T	ENSP00000385679.1:p.Gly121=
ENST00000407332.6:c.450C>T	ENSP00000384457.2:p.Gly150=
ENST00000407623.8:c.363C>T	ENSP00000384834.3:p.Gly121=
ENST00000438270.2:c.363C>T	ENSP00000403439.2:p.Gly121=
ENST00000684963.1:n.1709C>T
ENST00000686129.1:c.363C>T	ENSP00000508623.1:p.Gly121=
ENST00000686523.1:c.*381C>T	ENSP00000508940.1:n.*381C>T
ENST00000687183.1:n.493C>T
ENST00000687198.1:c.363C>T	ENSP00000508492.1:p.Gly121=
ENST00000688117.1:c.531C>T	ENSP00000509015.1:p.Gly177=
ENST00000688244.1:c.333+2699C>T	ENSP00000510355.1:n.333+2699C>T
ENST00000689001.1:n.839C>T
ENST00000689195.1:c.432C>T	ENSP00000509895.1:p.Gly144=
ENST00000689239.1:n.599C>T
ENST00000689795.1:n.594C>T
ENST00000690835.1:c.432C>T	ENSP00000509038.1:p.Gly144=
ENST00000690993.1:n.509C>T
ENST00000691295.1:c.334-495C>T	ENSP00000508706.1:n.334-495C>T
ENST00000691918.1:c.411C>T	ENSP00000509525.1:p.Gly137=
ENST00000692152.1:c.363C>T	ENSP00000509317.1:p.Gly121=
ENST00000692344.1:n.456C>T
ENST00000693157.1:c.352C>T	ENSP00000510610.1:n.352C>T
ENST00000693363.1:c.432C>T	ENSP00000510411.1:p.Gly144=
ENST00000693367.1:c.432C>T	ENSP00000508815.1:p.Gly144=
ENST00000693639.1:c.425C>T	ENSP00000510223.1:p.Ala142Val
ENST00000693646.1:c.338C>T	ENSP00000508449.1:p.Ala113Val
ENST00000352397.10:c.432C>T MANE Select	ENSP00000338461.6:p.Gly144=
ENST00000352397.9:c.432C>T	ENSP00000338461.6:p.Gly144=
ENST00000361740.8:c.531C>T	ENSP00000354468.4:p.Gly177=
ENST00000402438.5:c.363C>T	ENSP00000385679.1:p.Gly121=
ENST00000407332.5:c.363C>T	ENSP00000384457.1:p.Gly121=
ENST00000407623.7:c.363C>T	ENSP00000384834.3:p.Gly121=
ENST00000438270.1:c.363C>T	ENSP00000403439.1:p.Gly121=
ENST00000470741.1:n.2566C>T
NM_000398.6:c.432C>T	NP_000389.1:p.Gly144=
NM_001129819.2:c.363C>T	NP_001123291.1:p.Gly121=
NM_001171660.1:c.531C>T	NP_001165131.1:p.Gly177=
NM_001171661.1:c.363C>T	NP_001165132.1:p.Gly121=
NM_007326.4:c.363C>T	NP_015565.1:p.Gly121=
NM_000398.7:c.432C>T MANE Select	NP_000389.1:p.Gly144=
NM_001171660.2:c.531C>T	NP_001165131.1:p.Gly177=