Canonical Allele Identifier: CA2406837431
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42628048A= , CM000684.2:g.42628048A= GRCh38
NC_000022.10:g.43024054A= , CM000684.1:g.43024054A= GRCh37
NC_000022.9:g.41353998A= NCBI36
NG_012194.1:g.26352T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.463+104T= ENSP00000354468.5:n.463+104T=
ENST00000402438.6:c.394+104T= ENSP00000385679.1:n.394+104T=
ENST00000407332.6:c.481+104T= ENSP00000384457.2:n.481+104T=
ENST00000407623.8:c.394+104T= ENSP00000384834.3:n.394+104T=
ENST00000438270.2:c.394+104T= ENSP00000403439.2:n.394+104T=
ENST00000684963.1:n.1844T=
ENST00000686523.1:c.*412+104T= ENSP00000508940.1:n.*412+104T=
ENST00000687183.1:n.524+104T=
ENST00000687198.1:c.394+104T= ENSP00000508492.1:n.394+104T=
ENST00000688117.1:c.562+104T= ENSP00000509015.1:n.562+104T=
ENST00000688244.1:c.333+2834T= ENSP00000510355.1:n.333+2834T=
ENST00000689001.1:n.870+104T=
ENST00000689195.1:c.463+104T= ENSP00000509895.1:n.463+104T=
ENST00000689239.1:n.630+104T=
ENST00000689795.1:n.625+104T=
ENST00000690835.1:c.463+104T= ENSP00000509038.1:n.463+104T=
ENST00000690993.1:n.644T=
ENST00000691295.1:c.334-360T= ENSP00000508706.1:n.334-360T=
ENST00000691918.1:c.442+104T= ENSP00000509525.1:n.442+104T=
ENST00000692152.1:c.394+104T= ENSP00000509317.1:n.394+104T=
ENST00000692344.1:n.591T=
ENST00000693363.1:c.463+104T= ENSP00000510411.1:n.463+104T=
ENST00000693367.1:c.463+104T= ENSP00000508815.1:n.463+104T=
ENST00000693639.1:c.456+104T= ENSP00000510223.1:n.456+104T=
ENST00000693646.1:c.369+104T= ENSP00000508449.1:n.369+104T=
ENST00000352397.10:c.463+104T= MANE Select ENSP00000338461.6:n.463+104T=
ENST00000352397.9:c.463+104T= ENSP00000338461.6:n.463+104T=
ENST00000361740.8:c.562+104T= ENSP00000354468.4:n.562+104T=
ENST00000402438.5:c.394+104T= ENSP00000385679.1:n.394+104T=
ENST00000407332.5:c.394+104T= ENSP00000384457.1:n.394+104T=
ENST00000407623.7:c.394+104T= ENSP00000384834.3:n.394+104T=
ENST00000438270.1:c.394+104T= ENSP00000403439.1:n.394+104T=
ENST00000470741.1:n.2597+104T=
NM_000398.6:c.463+104T= NP_000389.1:n.463+104T=
NM_001129819.2:c.394+104T= NP_001123291.1:n.394+104T=
NM_001171660.1:c.562+104T= NP_001165131.1:n.562+104T=
NM_001171661.1:c.394+104T= NP_001165132.1:n.394+104T=
NM_007326.4:c.394+104T= NP_015565.1:n.394+104T=
NM_000398.7:c.463+104T= MANE Select NP_000389.1:n.463+104T=
NM_001171660.2:c.562+104T= NP_001165131.1:n.562+104T=