Canonical Allele Identifier: CA2406835198
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42623865T= , CM000684.2:g.42623865T= GRCh38
NC_000022.10:g.43019871T= , CM000684.1:g.43019871T= GRCh37
NC_000022.9:g.41349815T= NCBI36
NG_012194.1:g.30535A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.789A= ENSP00000354468.5:p.Arg263=
ENST00000402438.6:c.588A= ENSP00000385679.1:p.Arg196=
ENST00000407332.6:c.675A= ENSP00000384457.2:p.Arg225=
ENST00000407623.8:c.588A= ENSP00000384834.3:p.Arg196=
ENST00000617178.5:c.194A=
ENST00000684963.1:n.2397A=
ENST00000685184.1:n.249A=
ENST00000686523.1:c.*606A= ENSP00000508940.1:n.*606A=
ENST00000687183.1:n.933A=
ENST00000687198.1:c.588A= ENSP00000508492.1:p.Arg196=
ENST00000688117.1:c.756A= ENSP00000509015.1:p.Arg252=
ENST00000688244.1:c.357A= ENSP00000510355.1:p.Arg119=
ENST00000689001.1:n.1279A=
ENST00000689195.1:c.573A= ENSP00000509895.1:p.Arg191=
ENST00000689239.1:n.824A=
ENST00000689795.1:n.918A=
ENST00000690835.1:c.*36A= ENSP00000509038.1:n.*36A=
ENST00000690993.1:n.1412A=
ENST00000691295.1:c.*140A= ENSP00000508706.1:n.*140A=
ENST00000691918.1:c.947A= ENSP00000509525.1:n.947A=
ENST00000692152.1:c.588A= ENSP00000509317.1:p.Arg196=
ENST00000692344.1:n.1144A=
ENST00000693363.1:c.699A= ENSP00000510411.1:p.Arg233=
ENST00000693367.1:c.657A= ENSP00000508815.1:p.Arg219=
ENST00000693639.1:c.650A= ENSP00000510223.1:n.650A=
ENST00000693646.1:c.563A= ENSP00000508449.1:n.563A=
ENST00000352397.10:c.657A= MANE Select ENSP00000338461.6:p.Arg219=
ENST00000352397.9:c.657A= ENSP00000338461.6:p.Arg219=
ENST00000361740.8:c.756A= ENSP00000354468.4:p.Arg252=
ENST00000402438.5:c.588A= ENSP00000385679.1:p.Arg196=
ENST00000407332.5:c.588A= ENSP00000384457.1:p.Arg196=
ENST00000407623.7:c.588A= ENSP00000384834.3:p.Arg196=
ENST00000470741.1:n.2791A=
NM_000398.6:c.657A= NP_000389.1:p.Arg219=
NM_001129819.2:c.588A= NP_001123291.1:p.Arg196=
NM_001171660.1:c.756A= NP_001165131.1:p.Arg252=
NM_001171661.1:c.588A= NP_001165132.1:p.Arg196=
NM_007326.4:c.588A= NP_015565.1:p.Arg196=
NM_000398.7:c.657A= MANE Select NP_000389.1:p.Arg219=
NM_001171660.2:c.756A= NP_001165131.1:p.Arg252=