Canonical Allele Identifier: CA2406835278
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42623999C= , CM000684.2:g.42623999C= GRCh38
NC_000022.10:g.43020005C= , CM000684.1:g.43020005C= GRCh37
NC_000022.9:g.41349949C= NCBI36
NG_012194.1:g.30401G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.766-111G= ENSP00000354468.5:n.766-111G=
ENST00000402438.6:c.565-111G= ENSP00000385679.1:n.565-111G=
ENST00000407332.6:c.652-111G= ENSP00000384457.2:n.652-111G=
ENST00000407623.8:c.565-111G= ENSP00000384834.3:n.565-111G=
ENST00000617178.5:c.171-111G=
ENST00000684963.1:n.2374-111G=
ENST00000685184.1:n.115G=
ENST00000686523.1:c.*583-111G= ENSP00000508940.1:n.*583-111G=
ENST00000687183.1:n.910-111G=
ENST00000687198.1:c.565-111G= ENSP00000508492.1:n.565-111G=
ENST00000688117.1:c.733-111G= ENSP00000509015.1:n.733-111G=
ENST00000688244.1:c.334-111G= ENSP00000510355.1:n.334-111G=
ENST00000689001.1:n.1256-111G=
ENST00000689195.1:c.550-111G= ENSP00000509895.1:n.550-111G=
ENST00000689239.1:n.801-111G=
ENST00000689795.1:n.895-111G=
ENST00000690835.1:c.*13-111G= ENSP00000509038.1:n.*13-111G=
ENST00000690993.1:n.1389-111G=
ENST00000691295.1:c.*117-111G= ENSP00000508706.1:n.*117-111G=
ENST00000691918.1:c.924-111G= ENSP00000509525.1:n.924-111G=
ENST00000692152.1:c.565-111G= ENSP00000509317.1:n.565-111G=
ENST00000692344.1:n.1121-111G=
ENST00000693363.1:c.676-111G= ENSP00000510411.1:n.676-111G=
ENST00000693367.1:c.634-111G= ENSP00000508815.1:n.634-111G=
ENST00000693639.1:c.627-111G= ENSP00000510223.1:n.627-111G=
ENST00000693646.1:c.540-111G= ENSP00000508449.1:n.540-111G=
ENST00000352397.10:c.634-111G= MANE Select ENSP00000338461.6:n.634-111G=
ENST00000352397.9:c.634-111G= ENSP00000338461.6:n.634-111G=
ENST00000361740.8:c.733-111G= ENSP00000354468.4:n.733-111G=
ENST00000402438.5:c.565-111G= ENSP00000385679.1:n.565-111G=
ENST00000407332.5:c.565-111G= ENSP00000384457.1:n.565-111G=
ENST00000407623.7:c.565-111G= ENSP00000384834.3:n.565-111G=
ENST00000470741.1:n.2768-111G=
NM_000398.6:c.634-111G= NP_000389.1:n.634-111G=
NM_001129819.2:c.565-111G= NP_001123291.1:n.565-111G=
NM_001171660.1:c.733-111G= NP_001165131.1:n.733-111G=
NM_001171661.1:c.565-111G= NP_001165132.1:n.565-111G=
NM_007326.4:c.565-111G= NP_015565.1:n.565-111G=
NM_000398.7:c.634-111G= MANE Select NP_000389.1:n.634-111G=
NM_001171660.2:c.733-111G= NP_001165131.1:n.733-111G=