Canonical Allele Identifier: CA324703200
Gene: CYB5R3 HGNC NCBI

Linked Data

dbSNP Id: rs1019340929

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42630956C>T , CM000684.2:g.42630956C>T GRCh38
NC_000022.10:g.43026962C>T , CM000684.1:g.43026962C>T GRCh37
NC_000022.9:g.41356906C>T NCBI36
NG_012194.1:g.23444G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.259G>A ENSP00000354468.5:p.Gly87Arg
ENST00000402438.6:c.190G>A ENSP00000385679.1:p.Gly64Arg
ENST00000407332.6:c.277G>A ENSP00000384457.2:p.Gly93Arg
ENST00000407623.8:c.190G>A ENSP00000384834.3:p.Gly64Arg
ENST00000438270.2:c.190G>A ENSP00000403439.2:p.Gly64Arg
ENST00000466276.2:n.326G>A
ENST00000686129.1:c.190G>A ENSP00000508623.1:p.Gly64Arg
ENST00000686523.1:c.*208G>A ENSP00000508940.1:n.*208G>A
ENST00000687183.1:n.320G>A
ENST00000687198.1:c.190G>A ENSP00000508492.1:p.Gly64Arg
ENST00000688117.1:c.358G>A ENSP00000509015.1:p.Gly120Arg
ENST00000688244.1:c.259G>A ENSP00000510355.1:p.Gly87Arg
ENST00000689001.1:n.666G>A
ENST00000689195.1:c.259G>A ENSP00000509895.1:p.Gly87Arg
ENST00000689239.1:n.426G>A
ENST00000689795.1:n.421G>A
ENST00000690835.1:c.259G>A ENSP00000509038.1:p.Gly87Arg
ENST00000690993.1:n.336G>A
ENST00000691295.1:c.259G>A ENSP00000508706.1:p.Gly87Arg
ENST00000691918.1:c.238G>A ENSP00000509525.1:p.Gly80Arg
ENST00000692152.1:c.190G>A ENSP00000509317.1:p.Gly64Arg
ENST00000692344.1:n.283G>A
ENST00000693157.1:c.179G>A ENSP00000510610.1:n.179G>A
ENST00000693363.1:c.259G>A ENSP00000510411.1:p.Gly87Arg
ENST00000693367.1:c.259G>A ENSP00000508815.1:p.Gly87Arg
ENST00000693639.1:c.252G>A ENSP00000510223.1:p.Met84Ile
ENST00000693646.1:c.165G>A ENSP00000508449.1:p.Met55Ile
ENST00000693716.1:n.487G>A
ENST00000352397.10:c.259G>A MANE Select ENSP00000338461.6:p.Gly87Arg
ENST00000352397.9:c.259G>A ENSP00000338461.6:p.Gly87Arg
ENST00000361740.8:c.358G>A ENSP00000354468.4:p.Gly120Arg
ENST00000402438.5:c.190G>A ENSP00000385679.1:p.Gly64Arg
ENST00000407332.5:c.190G>A ENSP00000384457.1:p.Gly64Arg
ENST00000407623.7:c.190G>A ENSP00000384834.3:p.Gly64Arg
ENST00000438270.1:c.190G>A ENSP00000403439.1:p.Gly64Arg
ENST00000470741.1:n.2393G>A
NM_000398.6:c.259G>A NP_000389.1:p.Gly87Arg
NM_001129819.2:c.190G>A NP_001123291.1:p.Gly64Arg
NM_001171660.1:c.358G>A NP_001165131.1:p.Gly120Arg
NM_001171661.1:c.190G>A NP_001165132.1:p.Gly64Arg
NM_007326.4:c.190G>A NP_015565.1:p.Gly64Arg
NM_000398.7:c.259G>A MANE Select NP_000389.1:p.Gly87Arg
NM_001171660.2:c.358G>A NP_001165131.1:p.Gly120Arg