Canonical Allele Identifier: CA2406839053

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42630899C= , CM000684.2:g.42630899C=	GRCh38
NC_000022.10:g.43026905C= , CM000684.1:g.43026905C=	GRCh37
NC_000022.9:g.41356849C=	NCBI36
NG_012194.1:g.23501G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.316G=	ENSP00000354468.5:p.Val106=
ENST00000402438.6:c.247G=	ENSP00000385679.1:p.Val83=
ENST00000407332.6:c.334G=	ENSP00000384457.2:p.Val112=
ENST00000407623.8:c.247G=	ENSP00000384834.3:p.Val83=
ENST00000438270.2:c.247G=	ENSP00000403439.2:p.Val83=
ENST00000466276.2:n.383G=
ENST00000686129.1:c.247G=	ENSP00000508623.1:p.Val83=
ENST00000686523.1:c.*265G=	ENSP00000508940.1:n.*265G=
ENST00000687183.1:n.377G=
ENST00000687198.1:c.247G=	ENSP00000508492.1:p.Val83=
ENST00000688117.1:c.415G=	ENSP00000509015.1:p.Val139=
ENST00000688244.1:c.316G=	ENSP00000510355.1:p.Val106=
ENST00000689001.1:n.723G=
ENST00000689195.1:c.316G=	ENSP00000509895.1:p.Val106=
ENST00000689239.1:n.483G=
ENST00000689795.1:n.478G=
ENST00000690835.1:c.316G=	ENSP00000509038.1:p.Val106=
ENST00000690993.1:n.393G=
ENST00000691295.1:c.316G=	ENSP00000508706.1:p.Val106=
ENST00000691918.1:c.295G=	ENSP00000509525.1:p.Val99=
ENST00000692152.1:c.247G=	ENSP00000509317.1:p.Val83=
ENST00000692344.1:n.340G=
ENST00000693157.1:c.236G=	ENSP00000510610.1:n.236G=
ENST00000693363.1:c.316G=	ENSP00000510411.1:p.Val106=
ENST00000693367.1:c.316G=	ENSP00000508815.1:p.Val106=
ENST00000693639.1:c.309G=	ENSP00000510223.1:p.Ser103=
ENST00000693646.1:c.222G=	ENSP00000508449.1:p.Ser74=
ENST00000693716.1:n.544G=
ENST00000352397.10:c.316G= MANE Select	ENSP00000338461.6:p.Val106=
ENST00000352397.9:c.316G=	ENSP00000338461.6:p.Val106=
ENST00000361740.8:c.415G=	ENSP00000354468.4:p.Val139=
ENST00000402438.5:c.247G=	ENSP00000385679.1:p.Val83=
ENST00000407332.5:c.247G=	ENSP00000384457.1:p.Val83=
ENST00000407623.7:c.247G=	ENSP00000384834.3:p.Val83=
ENST00000438270.1:c.247G=	ENSP00000403439.1:p.Val83=
ENST00000470741.1:n.2450G=
NM_000398.6:c.316G=	NP_000389.1:p.Val106=
NM_001129819.2:c.247G=	NP_001123291.1:p.Val83=
NM_001171660.1:c.415G=	NP_001165131.1:p.Val139=
NM_001171661.1:c.247G=	NP_001165132.1:p.Val83=
NM_007326.4:c.247G=	NP_015565.1:p.Val83=
NM_000398.7:c.316G= MANE Select	NP_000389.1:p.Val106=
NM_001171660.2:c.415G=	NP_001165131.1:p.Val139=