Canonical Allele Identifier: CA2406835177
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42623812T= , CM000684.2:g.42623812T= GRCh38
NC_000022.10:g.43019818T= , CM000684.1:g.43019818T= GRCh37
NC_000022.9:g.41349762T= NCBI36
NG_012194.1:g.30588A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.842A= ENSP00000354468.5:p.Tyr281=
ENST00000402438.6:c.641A= ENSP00000385679.1:p.Tyr214=
ENST00000407332.6:c.728A= ENSP00000384457.2:p.Tyr243=
ENST00000407623.8:c.641A= ENSP00000384834.3:p.Tyr214=
ENST00000617178.5:c.247A=
ENST00000684963.1:n.2450A=
ENST00000685184.1:n.302A=
ENST00000686523.1:c.*659A= ENSP00000508940.1:n.*659A=
ENST00000687183.1:n.986A=
ENST00000687198.1:c.641A= ENSP00000508492.1:p.Tyr214=
ENST00000688117.1:c.809A= ENSP00000509015.1:p.Tyr270=
ENST00000688244.1:c.410A= ENSP00000510355.1:p.Tyr137=
ENST00000689001.1:n.1332A=
ENST00000689195.1:c.626A= ENSP00000509895.1:p.Tyr209=
ENST00000689239.1:n.877A=
ENST00000689795.1:n.971A=
ENST00000690835.1:c.*89A= ENSP00000509038.1:n.*89A=
ENST00000690993.1:n.1465A=
ENST00000691295.1:c.*193A= ENSP00000508706.1:n.*193A=
ENST00000691918.1:c.1000A= ENSP00000509525.1:n.1000A=
ENST00000692152.1:c.641A= ENSP00000509317.1:p.Tyr214=
ENST00000692344.1:n.1197A=
ENST00000693363.1:c.752A= ENSP00000510411.1:p.Tyr251=
ENST00000693367.1:c.710A= ENSP00000508815.1:p.Tyr237=
ENST00000693639.1:c.703A= ENSP00000510223.1:n.703A=
ENST00000693646.1:c.616A= ENSP00000508449.1:n.616A=
ENST00000352397.10:c.710A= MANE Select ENSP00000338461.6:p.Tyr237=
ENST00000352397.9:c.710A= ENSP00000338461.6:p.Tyr237=
ENST00000361740.8:c.809A= ENSP00000354468.4:p.Tyr270=
ENST00000402438.5:c.641A= ENSP00000385679.1:p.Tyr214=
ENST00000407332.5:c.641A= ENSP00000384457.1:p.Tyr214=
ENST00000407623.7:c.641A= ENSP00000384834.3:p.Tyr214=
ENST00000470741.1:n.2844A=
NM_000398.6:c.710A= NP_000389.1:p.Tyr237=
NM_001129819.2:c.641A= NP_001123291.1:p.Tyr214=
NM_001171660.1:c.809A= NP_001165131.1:p.Tyr270=
NM_001171661.1:c.641A= NP_001165132.1:p.Tyr214=
NM_007326.4:c.641A= NP_015565.1:p.Tyr214=
NM_000398.7:c.710A= MANE Select NP_000389.1:p.Tyr237=
NM_001171660.2:c.809A= NP_001165131.1:p.Tyr270=