Canonical Allele Identifier: CA2406839066
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42630922G= , CM000684.2:g.42630922G= GRCh38
NC_000022.10:g.43026928G= , CM000684.1:g.43026928G= GRCh37
NC_000022.9:g.41356872G= NCBI36
NG_012194.1:g.23478C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.293C= ENSP00000354468.5:p.Ser98=
ENST00000402438.6:c.224C= ENSP00000385679.1:p.Ser75=
ENST00000407332.6:c.311C= ENSP00000384457.2:p.Ser104=
ENST00000407623.8:c.224C= ENSP00000384834.3:p.Ser75=
ENST00000438270.2:c.224C= ENSP00000403439.2:p.Ser75=
ENST00000466276.2:n.360C=
ENST00000686129.1:c.224C= ENSP00000508623.1:p.Ser75=
ENST00000686523.1:c.*242C= ENSP00000508940.1:n.*242C=
ENST00000687183.1:n.354C=
ENST00000687198.1:c.224C= ENSP00000508492.1:p.Ser75=
ENST00000688117.1:c.392C= ENSP00000509015.1:p.Ser131=
ENST00000688244.1:c.293C= ENSP00000510355.1:p.Ser98=
ENST00000689001.1:n.700C=
ENST00000689195.1:c.293C= ENSP00000509895.1:p.Ser98=
ENST00000689239.1:n.460C=
ENST00000689795.1:n.455C=
ENST00000690835.1:c.293C= ENSP00000509038.1:p.Ser98=
ENST00000690993.1:n.370C=
ENST00000691295.1:c.293C= ENSP00000508706.1:p.Ser98=
ENST00000691918.1:c.272C= ENSP00000509525.1:p.Ser91=
ENST00000692152.1:c.224C= ENSP00000509317.1:p.Ser75=
ENST00000692344.1:n.317C=
ENST00000693157.1:c.213C= ENSP00000510610.1:n.213C=
ENST00000693363.1:c.293C= ENSP00000510411.1:p.Ser98=
ENST00000693367.1:c.293C= ENSP00000508815.1:p.Ser98=
ENST00000693639.1:c.286C= ENSP00000510223.1:p.Pro96=
ENST00000693646.1:c.199C= ENSP00000508449.1:p.Pro67=
ENST00000693716.1:n.521C=
ENST00000352397.10:c.293C= MANE Select ENSP00000338461.6:p.Ser98=
ENST00000352397.9:c.293C= ENSP00000338461.6:p.Ser98=
ENST00000361740.8:c.392C= ENSP00000354468.4:p.Ser131=
ENST00000402438.5:c.224C= ENSP00000385679.1:p.Ser75=
ENST00000407332.5:c.224C= ENSP00000384457.1:p.Ser75=
ENST00000407623.7:c.224C= ENSP00000384834.3:p.Ser75=
ENST00000438270.1:c.224C= ENSP00000403439.1:p.Ser75=
ENST00000470741.1:n.2427C=
NM_000398.6:c.293C= NP_000389.1:p.Ser98=
NM_001129819.2:c.224C= NP_001123291.1:p.Ser75=
NM_001171660.1:c.392C= NP_001165131.1:p.Ser131=
NM_001171661.1:c.224C= NP_001165132.1:p.Ser75=
NM_007326.4:c.224C= NP_015565.1:p.Ser75=
NM_000398.7:c.293C= MANE Select NP_000389.1:p.Ser98=
NM_001171660.2:c.392C= NP_001165131.1:p.Ser131=