Canonical Allele Identifier: CA2406835190
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42623833G= , CM000684.2:g.42623833G= GRCh38
NC_000022.10:g.43019839G= , CM000684.1:g.43019839G= GRCh37
NC_000022.9:g.41349783G= NCBI36
NG_012194.1:g.30567C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.821C= ENSP00000354468.5:p.Ser274=
ENST00000402438.6:c.620C= ENSP00000385679.1:p.Ser207=
ENST00000407332.6:c.707C= ENSP00000384457.2:p.Ser236=
ENST00000407623.8:c.620C= ENSP00000384834.3:p.Ser207=
ENST00000617178.5:c.226C=
ENST00000684963.1:n.2429C=
ENST00000685184.1:n.281C=
ENST00000686523.1:c.*638C= ENSP00000508940.1:n.*638C=
ENST00000687183.1:n.965C=
ENST00000687198.1:c.620C= ENSP00000508492.1:p.Ser207=
ENST00000688117.1:c.788C= ENSP00000509015.1:p.Ser263=
ENST00000688244.1:c.389C= ENSP00000510355.1:p.Ser130=
ENST00000689001.1:n.1311C=
ENST00000689195.1:c.605C= ENSP00000509895.1:p.Ser202=
ENST00000689239.1:n.856C=
ENST00000689795.1:n.950C=
ENST00000690835.1:c.*68C= ENSP00000509038.1:n.*68C=
ENST00000690993.1:n.1444C=
ENST00000691295.1:c.*172C= ENSP00000508706.1:n.*172C=
ENST00000691918.1:c.979C= ENSP00000509525.1:n.979C=
ENST00000692152.1:c.620C= ENSP00000509317.1:p.Ser207=
ENST00000692344.1:n.1176C=
ENST00000693363.1:c.731C= ENSP00000510411.1:p.Ser244=
ENST00000693367.1:c.689C= ENSP00000508815.1:p.Ser230=
ENST00000693639.1:c.682C= ENSP00000510223.1:n.682C=
ENST00000693646.1:c.595C= ENSP00000508449.1:n.595C=
ENST00000352397.10:c.689C= MANE Select ENSP00000338461.6:p.Ser230=
ENST00000352397.9:c.689C= ENSP00000338461.6:p.Ser230=
ENST00000361740.8:c.788C= ENSP00000354468.4:p.Ser263=
ENST00000402438.5:c.620C= ENSP00000385679.1:p.Ser207=
ENST00000407332.5:c.620C= ENSP00000384457.1:p.Ser207=
ENST00000407623.7:c.620C= ENSP00000384834.3:p.Ser207=
ENST00000470741.1:n.2823C=
NM_000398.6:c.689C= NP_000389.1:p.Ser230=
NM_001129819.2:c.620C= NP_001123291.1:p.Ser207=
NM_001171660.1:c.788C= NP_001165131.1:p.Ser263=
NM_001171661.1:c.620C= NP_001165132.1:p.Ser207=
NM_007326.4:c.620C= NP_015565.1:p.Ser207=
NM_000398.7:c.689C= MANE Select NP_000389.1:p.Ser230=
NM_001171660.2:c.788C= NP_001165131.1:p.Ser263=