Canonical Allele Identifier: CA2406836981
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42627350T= , CM000684.2:g.42627350T= GRCh38
NC_000022.10:g.43023356T= , CM000684.1:g.43023356T= GRCh37
NC_000022.9:g.41353300T= NCBI36
NG_012194.1:g.27050A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.719A= ENSP00000354468.5:p.Lys240=
ENST00000402438.6:c.518A= ENSP00000385679.1:p.Lys173=
ENST00000407332.6:c.605A= ENSP00000384457.2:p.Lys202=
ENST00000407623.8:c.518A= ENSP00000384834.3:p.Lys173=
ENST00000617178.5:c.124A=
ENST00000684963.1:n.2327A=
ENST00000686523.1:c.*536A= ENSP00000508940.1:n.*536A=
ENST00000687183.1:n.863A=
ENST00000687198.1:c.518A= ENSP00000508492.1:p.Lys173=
ENST00000688117.1:c.686A= ENSP00000509015.1:p.Lys229=
ENST00000688244.1:c.334-3462A= ENSP00000510355.1:n.334-3462A=
ENST00000689001.1:n.1209A=
ENST00000689195.1:c.503A= ENSP00000509895.1:p.Lys168=
ENST00000689239.1:n.754A=
ENST00000689795.1:n.749A=
ENST00000690835.1:c.587A= ENSP00000509038.1:p.Lys196=
ENST00000690993.1:n.1342A=
ENST00000691295.1:c.*70A= ENSP00000508706.1:n.*70A=
ENST00000691918.1:c.566A= ENSP00000509525.1:p.Lys189=
ENST00000692152.1:c.518A= ENSP00000509317.1:p.Lys173=
ENST00000692344.1:n.1074A=
ENST00000693363.1:c.629A= ENSP00000510411.1:p.Lys210=
ENST00000693367.1:c.587A= ENSP00000508815.1:p.Lys196=
ENST00000693639.1:c.580A= ENSP00000510223.1:n.580A=
ENST00000693646.1:c.493A= ENSP00000508449.1:n.493A=
ENST00000352397.10:c.587A= MANE Select ENSP00000338461.6:p.Lys196=
ENST00000352397.9:c.587A= ENSP00000338461.6:p.Lys196=
ENST00000361740.8:c.686A= ENSP00000354468.4:p.Lys229=
ENST00000402438.5:c.518A= ENSP00000385679.1:p.Lys173=
ENST00000407332.5:c.518A= ENSP00000384457.1:p.Lys173=
ENST00000407623.7:c.518A= ENSP00000384834.3:p.Lys173=
ENST00000470741.1:n.2721A=
NM_000398.6:c.587A= NP_000389.1:p.Lys196=
NM_001129819.2:c.518A= NP_001123291.1:p.Lys173=
NM_001171660.1:c.686A= NP_001165131.1:p.Lys229=
NM_001171661.1:c.518A= NP_001165132.1:p.Lys173=
NM_007326.4:c.518A= NP_015565.1:p.Lys173=
NM_000398.7:c.587A= MANE Select NP_000389.1:p.Lys196=
NM_001171660.2:c.686A= NP_001165131.1:p.Lys229=