Canonical Allele Identifier: CA2406837515
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42628161G= , CM000684.2:g.42628161G= GRCh38
NC_000022.10:g.43024167G= , CM000684.1:g.43024167G= GRCh37
NC_000022.9:g.41354111G= NCBI36
NG_012194.1:g.26239C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.454C= ENSP00000354468.5:p.Gln152=
ENST00000402438.6:c.385C= ENSP00000385679.1:p.Gln129=
ENST00000407332.6:c.472C= ENSP00000384457.2:p.Gln158=
ENST00000407623.8:c.385C= ENSP00000384834.3:p.Gln129=
ENST00000438270.2:c.385C= ENSP00000403439.2:p.Gln129=
ENST00000684963.1:n.1731C=
ENST00000686129.1:c.385C= ENSP00000508623.1:p.Gln129=
ENST00000686523.1:c.*403C= ENSP00000508940.1:n.*403C=
ENST00000687183.1:n.515C=
ENST00000687198.1:c.385C= ENSP00000508492.1:p.Gln129=
ENST00000688117.1:c.553C= ENSP00000509015.1:p.Gln185=
ENST00000688244.1:c.333+2721C= ENSP00000510355.1:n.333+2721C=
ENST00000689001.1:n.861C=
ENST00000689195.1:c.454C= ENSP00000509895.1:p.Gln152=
ENST00000689239.1:n.621C=
ENST00000689795.1:n.616C=
ENST00000690835.1:c.454C= ENSP00000509038.1:p.Gln152=
ENST00000690993.1:n.531C=
ENST00000691295.1:c.334-473C= ENSP00000508706.1:n.334-473C=
ENST00000691918.1:c.433C= ENSP00000509525.1:p.Gln145=
ENST00000692152.1:c.385C= ENSP00000509317.1:p.Gln129=
ENST00000692344.1:n.478C=
ENST00000693157.1:c.374C= ENSP00000510610.1:n.374C=
ENST00000693363.1:c.454C= ENSP00000510411.1:p.Gln152=
ENST00000693367.1:c.454C= ENSP00000508815.1:p.Gln152=
ENST00000693639.1:c.447C= ENSP00000510223.1:p.Thr149=
ENST00000693646.1:c.360C= ENSP00000508449.1:p.Thr120=
ENST00000352397.10:c.454C= MANE Select ENSP00000338461.6:p.Gln152=
ENST00000352397.9:c.454C= ENSP00000338461.6:p.Gln152=
ENST00000361740.8:c.553C= ENSP00000354468.4:p.Gln185=
ENST00000402438.5:c.385C= ENSP00000385679.1:p.Gln129=
ENST00000407332.5:c.385C= ENSP00000384457.1:p.Gln129=
ENST00000407623.7:c.385C= ENSP00000384834.3:p.Gln129=
ENST00000438270.1:c.385C= ENSP00000403439.1:p.Gln129=
ENST00000470741.1:n.2588C=
NM_000398.6:c.454C= NP_000389.1:p.Gln152=
NM_001129819.2:c.385C= NP_001123291.1:p.Gln129=
NM_001171660.1:c.553C= NP_001165131.1:p.Gln185=
NM_001171661.1:c.385C= NP_001165132.1:p.Gln129=
NM_007326.4:c.385C= NP_015565.1:p.Gln129=
NM_000398.7:c.454C= MANE Select NP_000389.1:p.Gln152=
NM_001171660.2:c.553C= NP_001165131.1:p.Gln185=