Canonical Allele Identifier: CA2406835174
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42623809G= , CM000684.2:g.42623809G= GRCh38
NC_000022.10:g.43019815G= , CM000684.1:g.43019815G= GRCh37
NC_000022.9:g.41349759G= NCBI36
NG_012194.1:g.30591C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.845C= ENSP00000354468.5:p.Thr282=
ENST00000402438.6:c.644C= ENSP00000385679.1:p.Thr215=
ENST00000407332.6:c.731C= ENSP00000384457.2:p.Thr244=
ENST00000407623.8:c.644C= ENSP00000384834.3:p.Thr215=
ENST00000617178.5:c.250C=
ENST00000684963.1:n.2453C=
ENST00000685184.1:n.305C=
ENST00000686523.1:c.*662C= ENSP00000508940.1:n.*662C=
ENST00000687183.1:n.989C=
ENST00000687198.1:c.644C= ENSP00000508492.1:p.Thr215=
ENST00000688117.1:c.812C= ENSP00000509015.1:p.Thr271=
ENST00000688244.1:c.413C= ENSP00000510355.1:p.Thr138=
ENST00000689001.1:n.1335C=
ENST00000689195.1:c.629C= ENSP00000509895.1:p.Thr210=
ENST00000689239.1:n.880C=
ENST00000689795.1:n.974C=
ENST00000690835.1:c.*92C= ENSP00000509038.1:n.*92C=
ENST00000690993.1:n.1468C=
ENST00000691295.1:c.*196C= ENSP00000508706.1:n.*196C=
ENST00000691918.1:c.1003C= ENSP00000509525.1:n.1003C=
ENST00000692152.1:c.644C= ENSP00000509317.1:p.Thr215=
ENST00000692344.1:n.1200C=
ENST00000693363.1:c.755C= ENSP00000510411.1:p.Thr252=
ENST00000693367.1:c.713C= ENSP00000508815.1:p.Thr238=
ENST00000693639.1:c.706C= ENSP00000510223.1:n.706C=
ENST00000693646.1:c.619C= ENSP00000508449.1:n.619C=
ENST00000352397.10:c.713C= MANE Select ENSP00000338461.6:p.Thr238=
ENST00000352397.9:c.713C= ENSP00000338461.6:p.Thr238=
ENST00000361740.8:c.812C= ENSP00000354468.4:p.Thr271=
ENST00000402438.5:c.644C= ENSP00000385679.1:p.Thr215=
ENST00000407332.5:c.644C= ENSP00000384457.1:p.Thr215=
ENST00000407623.7:c.644C= ENSP00000384834.3:p.Thr215=
ENST00000470741.1:n.2847C=
NM_000398.6:c.713C= NP_000389.1:p.Thr238=
NM_001129819.2:c.644C= NP_001123291.1:p.Thr215=
NM_001171660.1:c.812C= NP_001165131.1:p.Thr271=
NM_001171661.1:c.644C= NP_001165132.1:p.Thr215=
NM_007326.4:c.644C= NP_015565.1:p.Thr215=
NM_000398.7:c.713C= MANE Select NP_000389.1:p.Thr238=
NM_001171660.2:c.812C= NP_001165131.1:p.Thr271=