Canonical Allele Identifier: CA2406839054
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42630902A= , CM000684.2:g.42630902A= GRCh38
NC_000022.10:g.43026908A= , CM000684.1:g.43026908A= GRCh37
NC_000022.9:g.41356852A= NCBI36
NG_012194.1:g.23498T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.313T= ENSP00000354468.5:p.Phe105=
ENST00000402438.6:c.244T= ENSP00000385679.1:p.Phe82=
ENST00000407332.6:c.331T= ENSP00000384457.2:p.Phe111=
ENST00000407623.8:c.244T= ENSP00000384834.3:p.Phe82=
ENST00000438270.2:c.244T= ENSP00000403439.2:p.Phe82=
ENST00000466276.2:n.380T=
ENST00000686129.1:c.244T= ENSP00000508623.1:p.Phe82=
ENST00000686523.1:c.*262T= ENSP00000508940.1:n.*262T=
ENST00000687183.1:n.374T=
ENST00000687198.1:c.244T= ENSP00000508492.1:p.Phe82=
ENST00000688117.1:c.412T= ENSP00000509015.1:p.Phe138=
ENST00000688244.1:c.313T= ENSP00000510355.1:p.Phe105=
ENST00000689001.1:n.720T=
ENST00000689195.1:c.313T= ENSP00000509895.1:p.Phe105=
ENST00000689239.1:n.480T=
ENST00000689795.1:n.475T=
ENST00000690835.1:c.313T= ENSP00000509038.1:p.Phe105=
ENST00000690993.1:n.390T=
ENST00000691295.1:c.313T= ENSP00000508706.1:p.Phe105=
ENST00000691918.1:c.292T= ENSP00000509525.1:p.Phe98=
ENST00000692152.1:c.244T= ENSP00000509317.1:p.Phe82=
ENST00000692344.1:n.337T=
ENST00000693157.1:c.233T= ENSP00000510610.1:n.233T=
ENST00000693363.1:c.313T= ENSP00000510411.1:p.Phe105=
ENST00000693367.1:c.313T= ENSP00000508815.1:p.Phe105=
ENST00000693639.1:c.306T= ENSP00000510223.1:p.Ala102=
ENST00000693646.1:c.219T= ENSP00000508449.1:p.Ala73=
ENST00000693716.1:n.541T=
ENST00000352397.10:c.313T= MANE Select ENSP00000338461.6:p.Phe105=
ENST00000352397.9:c.313T= ENSP00000338461.6:p.Phe105=
ENST00000361740.8:c.412T= ENSP00000354468.4:p.Phe138=
ENST00000402438.5:c.244T= ENSP00000385679.1:p.Phe82=
ENST00000407332.5:c.244T= ENSP00000384457.1:p.Phe82=
ENST00000407623.7:c.244T= ENSP00000384834.3:p.Phe82=
ENST00000438270.1:c.244T= ENSP00000403439.1:p.Phe82=
ENST00000470741.1:n.2447T=
NM_000398.6:c.313T= NP_000389.1:p.Phe105=
NM_001129819.2:c.244T= NP_001123291.1:p.Phe82=
NM_001171660.1:c.412T= NP_001165131.1:p.Phe138=
NM_001171661.1:c.244T= NP_001165132.1:p.Phe82=
NM_007326.4:c.244T= NP_015565.1:p.Phe82=
NM_000398.7:c.313T= MANE Select NP_000389.1:p.Phe105=
NM_001171660.2:c.412T= NP_001165131.1:p.Phe138=