Canonical Allele Identifier: CA2406837582
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42628264G= , CM000684.2:g.42628264G= GRCh38
NC_000022.10:g.43024270G= , CM000684.1:g.43024270G= GRCh37
NC_000022.9:g.41354214G= NCBI36
NG_012194.1:g.26136C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.351C= ENSP00000354468.5:p.Thr117=
ENST00000402438.6:c.282C= ENSP00000385679.1:p.Thr94=
ENST00000407332.6:c.369C= ENSP00000384457.2:p.Thr123=
ENST00000407623.8:c.282C= ENSP00000384834.3:p.Thr94=
ENST00000438270.2:c.282C= ENSP00000403439.2:p.Thr94=
ENST00000684963.1:n.1628C=
ENST00000686129.1:c.282C= ENSP00000508623.1:p.Thr94=
ENST00000686523.1:c.*300C= ENSP00000508940.1:n.*300C=
ENST00000687183.1:n.412C=
ENST00000687198.1:c.282C= ENSP00000508492.1:p.Thr94=
ENST00000688117.1:c.450C= ENSP00000509015.1:p.Thr150=
ENST00000688244.1:c.333+2618C= ENSP00000510355.1:n.333+2618C=
ENST00000689001.1:n.758C=
ENST00000689195.1:c.351C= ENSP00000509895.1:p.Thr117=
ENST00000689239.1:n.518C=
ENST00000689795.1:n.513C=
ENST00000690835.1:c.351C= ENSP00000509038.1:p.Thr117=
ENST00000690993.1:n.428C=
ENST00000691295.1:c.334-576C= ENSP00000508706.1:n.334-576C=
ENST00000691918.1:c.330C= ENSP00000509525.1:p.Thr110=
ENST00000692152.1:c.282C= ENSP00000509317.1:p.Thr94=
ENST00000692344.1:n.375C=
ENST00000693157.1:c.271C= ENSP00000510610.1:n.271C=
ENST00000693363.1:c.351C= ENSP00000510411.1:p.Thr117=
ENST00000693367.1:c.351C= ENSP00000508815.1:p.Thr117=
ENST00000693639.1:c.344C= ENSP00000510223.1:p.Pro115=
ENST00000693646.1:c.257C= ENSP00000508449.1:p.Pro86=
ENST00000352397.10:c.351C= MANE Select ENSP00000338461.6:p.Thr117=
ENST00000352397.9:c.351C= ENSP00000338461.6:p.Thr117=
ENST00000361740.8:c.450C= ENSP00000354468.4:p.Thr150=
ENST00000402438.5:c.282C= ENSP00000385679.1:p.Thr94=
ENST00000407332.5:c.282C= ENSP00000384457.1:p.Thr94=
ENST00000407623.7:c.282C= ENSP00000384834.3:p.Thr94=
ENST00000438270.1:c.282C= ENSP00000403439.1:p.Thr94=
ENST00000470741.1:n.2485C=
NM_000398.6:c.351C= NP_000389.1:p.Thr117=
NM_001129819.2:c.282C= NP_001123291.1:p.Thr94=
NM_001171660.1:c.450C= NP_001165131.1:p.Thr150=
NM_001171661.1:c.282C= NP_001165132.1:p.Thr94=
NM_007326.4:c.282C= NP_015565.1:p.Thr94=
NM_000398.7:c.351C= MANE Select NP_000389.1:p.Thr117=
NM_001171660.2:c.450C= NP_001165131.1:p.Thr150=