Canonical Allele Identifier: CA2406837571

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42628249G= , CM000684.2:g.42628249G=	GRCh38
NC_000022.10:g.43024255G= , CM000684.1:g.43024255G=	GRCh37
NC_000022.9:g.41354199G=	NCBI36
NG_012194.1:g.26151C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.366C=	ENSP00000354468.5:p.Pro122=
ENST00000402438.6:c.297C=	ENSP00000385679.1:p.Pro99=
ENST00000407332.6:c.384C=	ENSP00000384457.2:p.Pro128=
ENST00000407623.8:c.297C=	ENSP00000384834.3:p.Pro99=
ENST00000438270.2:c.297C=	ENSP00000403439.2:p.Pro99=
ENST00000684963.1:n.1643C=
ENST00000686129.1:c.297C=	ENSP00000508623.1:p.Pro99=
ENST00000686523.1:c.*315C=	ENSP00000508940.1:n.*315C=
ENST00000687183.1:n.427C=
ENST00000687198.1:c.297C=	ENSP00000508492.1:p.Pro99=
ENST00000688117.1:c.465C=	ENSP00000509015.1:p.Pro155=
ENST00000688244.1:c.333+2633C=	ENSP00000510355.1:n.333+2633C=
ENST00000689001.1:n.773C=
ENST00000689195.1:c.366C=	ENSP00000509895.1:p.Pro122=
ENST00000689239.1:n.533C=
ENST00000689795.1:n.528C=
ENST00000690835.1:c.366C=	ENSP00000509038.1:p.Pro122=
ENST00000690993.1:n.443C=
ENST00000691295.1:c.334-561C=	ENSP00000508706.1:n.334-561C=
ENST00000691918.1:c.345C=	ENSP00000509525.1:p.Pro115=
ENST00000692152.1:c.297C=	ENSP00000509317.1:p.Pro99=
ENST00000692344.1:n.390C=
ENST00000693157.1:c.286C=	ENSP00000510610.1:n.286C=
ENST00000693363.1:c.366C=	ENSP00000510411.1:p.Pro122=
ENST00000693367.1:c.366C=	ENSP00000508815.1:p.Pro122=
ENST00000693639.1:c.359C=	ENSP00000510223.1:p.Pro120=
ENST00000693646.1:c.272C=	ENSP00000508449.1:p.Pro91=
ENST00000352397.10:c.366C= MANE Select	ENSP00000338461.6:p.Pro122=
ENST00000352397.9:c.366C=	ENSP00000338461.6:p.Pro122=
ENST00000361740.8:c.465C=	ENSP00000354468.4:p.Pro155=
ENST00000402438.5:c.297C=	ENSP00000385679.1:p.Pro99=
ENST00000407332.5:c.297C=	ENSP00000384457.1:p.Pro99=
ENST00000407623.7:c.297C=	ENSP00000384834.3:p.Pro99=
ENST00000438270.1:c.297C=	ENSP00000403439.1:p.Pro99=
ENST00000470741.1:n.2500C=
NM_000398.6:c.366C=	NP_000389.1:p.Pro122=
NM_001129819.2:c.297C=	NP_001123291.1:p.Pro99=
NM_001171660.1:c.465C=	NP_001165131.1:p.Pro155=
NM_001171661.1:c.297C=	NP_001165132.1:p.Pro99=
NM_007326.4:c.297C=	NP_015565.1:p.Pro99=
NM_000398.7:c.366C= MANE Select	NP_000389.1:p.Pro122=
NM_001171660.2:c.465C=	NP_001165131.1:p.Pro155=