Canonical Allele Identifier: CA2406835181
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42623820C= , CM000684.2:g.42623820C= GRCh38
NC_000022.10:g.43019826C= , CM000684.1:g.43019826C= GRCh37
NC_000022.9:g.41349770C= NCBI36
NG_012194.1:g.30580G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.834G= ENSP00000354468.5:p.Lys278=
ENST00000402438.6:c.633G= ENSP00000385679.1:p.Lys211=
ENST00000407332.6:c.720G= ENSP00000384457.2:p.Lys240=
ENST00000407623.8:c.633G= ENSP00000384834.3:p.Lys211=
ENST00000617178.5:c.239G=
ENST00000684963.1:n.2442G=
ENST00000685184.1:n.294G=
ENST00000686523.1:c.*651G= ENSP00000508940.1:n.*651G=
ENST00000687183.1:n.978G=
ENST00000687198.1:c.633G= ENSP00000508492.1:p.Lys211=
ENST00000688117.1:c.801G= ENSP00000509015.1:p.Lys267=
ENST00000688244.1:c.402G= ENSP00000510355.1:p.Lys134=
ENST00000689001.1:n.1324G=
ENST00000689195.1:c.618G= ENSP00000509895.1:p.Lys206=
ENST00000689239.1:n.869G=
ENST00000689795.1:n.963G=
ENST00000690835.1:c.*81G= ENSP00000509038.1:n.*81G=
ENST00000690993.1:n.1457G=
ENST00000691295.1:c.*185G= ENSP00000508706.1:n.*185G=
ENST00000691918.1:c.992G= ENSP00000509525.1:n.992G=
ENST00000692152.1:c.633G= ENSP00000509317.1:p.Lys211=
ENST00000692344.1:n.1189G=
ENST00000693363.1:c.744G= ENSP00000510411.1:p.Lys248=
ENST00000693367.1:c.702G= ENSP00000508815.1:p.Lys234=
ENST00000693639.1:c.695G= ENSP00000510223.1:n.695G=
ENST00000693646.1:c.608G= ENSP00000508449.1:n.608G=
ENST00000352397.10:c.702G= MANE Select ENSP00000338461.6:p.Lys234=
ENST00000352397.9:c.702G= ENSP00000338461.6:p.Lys234=
ENST00000361740.8:c.801G= ENSP00000354468.4:p.Lys267=
ENST00000402438.5:c.633G= ENSP00000385679.1:p.Lys211=
ENST00000407332.5:c.633G= ENSP00000384457.1:p.Lys211=
ENST00000407623.7:c.633G= ENSP00000384834.3:p.Lys211=
ENST00000470741.1:n.2836G=
NM_000398.6:c.702G= NP_000389.1:p.Lys234=
NM_001129819.2:c.633G= NP_001123291.1:p.Lys211=
NM_001171660.1:c.801G= NP_001165131.1:p.Lys267=
NM_001171661.1:c.633G= NP_001165132.1:p.Lys211=
NM_007326.4:c.633G= NP_015565.1:p.Lys211=
NM_000398.7:c.702G= MANE Select NP_000389.1:p.Lys234=
NM_001171660.2:c.801G= NP_001165131.1:p.Lys267=