Canonical Allele Identifier: CA2406837530
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42628186C= , CM000684.2:g.42628186C= GRCh38
NC_000022.10:g.43024192C= , CM000684.1:g.43024192C= GRCh37
NC_000022.9:g.41354136C= NCBI36
NG_012194.1:g.26214G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.429G= ENSP00000354468.5:p.Arg143=
ENST00000402438.6:c.360G= ENSP00000385679.1:p.Arg120=
ENST00000407332.6:c.447G= ENSP00000384457.2:p.Arg149=
ENST00000407623.8:c.360G= ENSP00000384834.3:p.Arg120=
ENST00000438270.2:c.360G= ENSP00000403439.2:p.Arg120=
ENST00000684963.1:n.1706G=
ENST00000686129.1:c.360G= ENSP00000508623.1:p.Arg120=
ENST00000686523.1:c.*378G= ENSP00000508940.1:n.*378G=
ENST00000687183.1:n.490G=
ENST00000687198.1:c.360G= ENSP00000508492.1:p.Arg120=
ENST00000688117.1:c.528G= ENSP00000509015.1:p.Arg176=
ENST00000688244.1:c.333+2696G= ENSP00000510355.1:n.333+2696G=
ENST00000689001.1:n.836G=
ENST00000689195.1:c.429G= ENSP00000509895.1:p.Arg143=
ENST00000689239.1:n.596G=
ENST00000689795.1:n.591G=
ENST00000690835.1:c.429G= ENSP00000509038.1:p.Arg143=
ENST00000690993.1:n.506G=
ENST00000691295.1:c.334-498G= ENSP00000508706.1:n.334-498G=
ENST00000691918.1:c.408G= ENSP00000509525.1:p.Arg136=
ENST00000692152.1:c.360G= ENSP00000509317.1:p.Arg120=
ENST00000692344.1:n.453G=
ENST00000693157.1:c.349G= ENSP00000510610.1:n.349G=
ENST00000693363.1:c.429G= ENSP00000510411.1:p.Arg143=
ENST00000693367.1:c.429G= ENSP00000508815.1:p.Arg143=
ENST00000693639.1:c.422G= ENSP00000510223.1:p.Gly141=
ENST00000693646.1:c.335G= ENSP00000508449.1:p.Gly112=
ENST00000352397.10:c.429G= MANE Select ENSP00000338461.6:p.Arg143=
ENST00000352397.9:c.429G= ENSP00000338461.6:p.Arg143=
ENST00000361740.8:c.528G= ENSP00000354468.4:p.Arg176=
ENST00000402438.5:c.360G= ENSP00000385679.1:p.Arg120=
ENST00000407332.5:c.360G= ENSP00000384457.1:p.Arg120=
ENST00000407623.7:c.360G= ENSP00000384834.3:p.Arg120=
ENST00000438270.1:c.360G= ENSP00000403439.1:p.Arg120=
ENST00000470741.1:n.2563G=
NM_000398.6:c.429G= NP_000389.1:p.Arg143=
NM_001129819.2:c.360G= NP_001123291.1:p.Arg120=
NM_001171660.1:c.528G= NP_001165131.1:p.Arg176=
NM_001171661.1:c.360G= NP_001165132.1:p.Arg120=
NM_007326.4:c.360G= NP_015565.1:p.Arg120=
NM_000398.7:c.429G= MANE Select NP_000389.1:p.Arg143=
NM_001171660.2:c.528G= NP_001165131.1:p.Arg176=