Canonical Allele Identifier: CA2406835192
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42623837G= , CM000684.2:g.42623837G= GRCh38
NC_000022.10:g.43019843G= , CM000684.1:g.43019843G= GRCh37
NC_000022.9:g.41349787G= NCBI36
NG_012194.1:g.30563C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.817C= ENSP00000354468.5:p.His273=
ENST00000402438.6:c.616C= ENSP00000385679.1:p.His206=
ENST00000407332.6:c.703C= ENSP00000384457.2:p.His235=
ENST00000407623.8:c.616C= ENSP00000384834.3:p.His206=
ENST00000617178.5:c.222C=
ENST00000684963.1:n.2425C=
ENST00000685184.1:n.277C=
ENST00000686523.1:c.*634C= ENSP00000508940.1:n.*634C=
ENST00000687183.1:n.961C=
ENST00000687198.1:c.616C= ENSP00000508492.1:p.His206=
ENST00000688117.1:c.784C= ENSP00000509015.1:p.His262=
ENST00000688244.1:c.385C= ENSP00000510355.1:p.His129=
ENST00000689001.1:n.1307C=
ENST00000689195.1:c.601C= ENSP00000509895.1:p.His201=
ENST00000689239.1:n.852C=
ENST00000689795.1:n.946C=
ENST00000690835.1:c.*64C= ENSP00000509038.1:n.*64C=
ENST00000690993.1:n.1440C=
ENST00000691295.1:c.*168C= ENSP00000508706.1:n.*168C=
ENST00000691918.1:c.975C= ENSP00000509525.1:n.975C=
ENST00000692152.1:c.616C= ENSP00000509317.1:p.His206=
ENST00000692344.1:n.1172C=
ENST00000693363.1:c.727C= ENSP00000510411.1:p.His243=
ENST00000693367.1:c.685C= ENSP00000508815.1:p.His229=
ENST00000693639.1:c.678C= ENSP00000510223.1:n.678C=
ENST00000693646.1:c.591C= ENSP00000508449.1:n.591C=
ENST00000352397.10:c.685C= MANE Select ENSP00000338461.6:p.His229=
ENST00000352397.9:c.685C= ENSP00000338461.6:p.His229=
ENST00000361740.8:c.784C= ENSP00000354468.4:p.His262=
ENST00000402438.5:c.616C= ENSP00000385679.1:p.His206=
ENST00000407332.5:c.616C= ENSP00000384457.1:p.His206=
ENST00000407623.7:c.616C= ENSP00000384834.3:p.His206=
ENST00000470741.1:n.2819C=
NM_000398.6:c.685C= NP_000389.1:p.His229=
NM_001129819.2:c.616C= NP_001123291.1:p.His206=
NM_001171660.1:c.784C= NP_001165131.1:p.His262=
NM_001171661.1:c.616C= NP_001165132.1:p.His206=
NM_007326.4:c.616C= NP_015565.1:p.His206=
NM_000398.7:c.685C= MANE Select NP_000389.1:p.His229=
NM_001171660.2:c.784C= NP_001165131.1:p.His262=