Canonical Allele Identifier: CA2406835172
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42623807G= , CM000684.2:g.42623807G= GRCh38
NC_000022.10:g.43019813G= , CM000684.1:g.43019813G= GRCh37
NC_000022.9:g.41349757G= NCBI36
NG_012194.1:g.30593C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.847C= ENSP00000354468.5:p.Leu283=
ENST00000402438.6:c.646C= ENSP00000385679.1:p.Leu216=
ENST00000407332.6:c.733C= ENSP00000384457.2:p.Leu245=
ENST00000407623.8:c.646C= ENSP00000384834.3:p.Leu216=
ENST00000617178.5:c.252C=
ENST00000684963.1:n.2455C=
ENST00000685184.1:n.307C=
ENST00000686523.1:c.*664C= ENSP00000508940.1:n.*664C=
ENST00000687183.1:n.991C=
ENST00000687198.1:c.646C= ENSP00000508492.1:p.Leu216=
ENST00000688117.1:c.814C= ENSP00000509015.1:p.Leu272=
ENST00000688244.1:c.415C= ENSP00000510355.1:p.Leu139=
ENST00000689001.1:n.1337C=
ENST00000689195.1:c.631C= ENSP00000509895.1:p.Leu211=
ENST00000689239.1:n.882C=
ENST00000689795.1:n.976C=
ENST00000690835.1:c.*94C= ENSP00000509038.1:n.*94C=
ENST00000690993.1:n.1470C=
ENST00000691295.1:c.*198C= ENSP00000508706.1:n.*198C=
ENST00000691918.1:c.1005C= ENSP00000509525.1:n.1005C=
ENST00000692152.1:c.646C= ENSP00000509317.1:p.Leu216=
ENST00000692344.1:n.1202C=
ENST00000693363.1:c.757C= ENSP00000510411.1:p.Leu253=
ENST00000693367.1:c.715C= ENSP00000508815.1:p.Leu239=
ENST00000693639.1:c.708C= ENSP00000510223.1:n.708C=
ENST00000693646.1:c.621C= ENSP00000508449.1:n.621C=
ENST00000352397.10:c.715C= MANE Select ENSP00000338461.6:p.Leu239=
ENST00000352397.9:c.715C= ENSP00000338461.6:p.Leu239=
ENST00000361740.8:c.814C= ENSP00000354468.4:p.Leu272=
ENST00000402438.5:c.646C= ENSP00000385679.1:p.Leu216=
ENST00000407332.5:c.646C= ENSP00000384457.1:p.Leu216=
ENST00000407623.7:c.646C= ENSP00000384834.3:p.Leu216=
ENST00000470741.1:n.2849C=
NM_000398.6:c.715C= NP_000389.1:p.Leu239=
NM_001129819.2:c.646C= NP_001123291.1:p.Leu216=
NM_001171660.1:c.814C= NP_001165131.1:p.Leu272=
NM_001171661.1:c.646C= NP_001165132.1:p.Leu216=
NM_007326.4:c.646C= NP_015565.1:p.Leu216=
NM_000398.7:c.715C= MANE Select NP_000389.1:p.Leu239=
NM_001171660.2:c.814C= NP_001165131.1:p.Leu272=