Canonical Allele Identifier: CA2406837152
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42627599G= , CM000684.2:g.42627599G= GRCh38
NC_000022.10:g.43023605G= , CM000684.1:g.43023605G= GRCh37
NC_000022.9:g.41353549G= NCBI36
NG_012194.1:g.26801C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361740.9:c.679+6C= ENSP00000354468.5:n.679+6C=
ENST00000402438.6:c.478+6C= ENSP00000385679.1:n.478+6C=
ENST00000407332.6:c.565+6C= ENSP00000384457.2:n.565+6C=
ENST00000407623.8:c.478+6C= ENSP00000384834.3:n.478+6C=
ENST00000617178.5:c.84+6C=
ENST00000684963.1:n.2287+6C=
ENST00000686523.1:c.*496+6C= ENSP00000508940.1:n.*496+6C=
ENST00000687183.1:n.614C=
ENST00000687198.1:c.478+6C= ENSP00000508492.1:n.478+6C=
ENST00000688117.1:c.646+6C= ENSP00000509015.1:n.646+6C=
ENST00000688244.1:c.333+3283C= ENSP00000510355.1:n.333+3283C=
ENST00000689001.1:n.960C=
ENST00000689195.1:c.464-210C= ENSP00000509895.1:n.464-210C=
ENST00000689239.1:n.714+6C=
ENST00000689795.1:n.709+6C=
ENST00000690835.1:c.547+6C= ENSP00000509038.1:n.547+6C=
ENST00000690993.1:n.1093C=
ENST00000691295.1:c.*30+6C= ENSP00000508706.1:n.*30+6C=
ENST00000691918.1:c.526+6C= ENSP00000509525.1:n.526+6C=
ENST00000692152.1:c.478+6C= ENSP00000509317.1:n.478+6C=
ENST00000692344.1:n.1034+6C=
ENST00000693363.1:c.547+6C= ENSP00000510411.1:n.547+6C=
ENST00000693367.1:c.547+6C= ENSP00000508815.1:n.547+6C=
ENST00000693639.1:c.540+6C= ENSP00000510223.1:n.540+6C=
ENST00000693646.1:c.453+6C= ENSP00000508449.1:n.453+6C=
ENST00000352397.10:c.547+6C= MANE Select ENSP00000338461.6:n.547+6C=
ENST00000352397.9:c.547+6C= ENSP00000338461.6:n.547+6C=
ENST00000361740.8:c.646+6C= ENSP00000354468.4:n.646+6C=
ENST00000402438.5:c.478+6C= ENSP00000385679.1:n.478+6C=
ENST00000407332.5:c.478+6C= ENSP00000384457.1:n.478+6C=
ENST00000407623.7:c.478+6C= ENSP00000384834.3:n.478+6C=
ENST00000470741.1:n.2681+6C=
NM_000398.6:c.547+6C= NP_000389.1:n.547+6C=
NM_001129819.2:c.478+6C= NP_001123291.1:n.478+6C=
NM_001171660.1:c.646+6C= NP_001165131.1:n.646+6C=
NM_001171661.1:c.478+6C= NP_001165132.1:n.478+6C=
NM_007326.4:c.478+6C= NP_015565.1:n.478+6C=
NM_000398.7:c.547+6C= MANE Select NP_000389.1:n.547+6C=
NM_001171660.2:c.646+6C= NP_001165131.1:n.646+6C=