Canonical Allele Identifier: CA2406839090
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42630961A= , CM000684.2:g.42630961A= GRCh38
NC_000022.10:g.43026967A= , CM000684.1:g.43026967A= GRCh37
NC_000022.9:g.41356911A= NCBI36
NG_012194.1:g.23439T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.254T= ENSP00000354468.5:p.Ile85=
ENST00000402438.6:c.185T= ENSP00000385679.1:p.Ile62=
ENST00000407332.6:c.272T= ENSP00000384457.2:p.Ile91=
ENST00000407623.8:c.185T= ENSP00000384834.3:p.Ile62=
ENST00000438270.2:c.185T= ENSP00000403439.2:p.Ile62=
ENST00000466276.2:n.321T=
ENST00000686129.1:c.185T= ENSP00000508623.1:p.Ile62=
ENST00000686523.1:c.*203T= ENSP00000508940.1:n.*203T=
ENST00000687183.1:n.315T=
ENST00000687198.1:c.185T= ENSP00000508492.1:p.Ile62=
ENST00000688117.1:c.353T= ENSP00000509015.1:p.Ile118=
ENST00000688244.1:c.254T= ENSP00000510355.1:p.Ile85=
ENST00000689001.1:n.661T=
ENST00000689195.1:c.254T= ENSP00000509895.1:p.Ile85=
ENST00000689239.1:n.421T=
ENST00000689795.1:n.416T=
ENST00000690835.1:c.254T= ENSP00000509038.1:p.Ile85=
ENST00000690993.1:n.331T=
ENST00000691295.1:c.254T= ENSP00000508706.1:p.Ile85=
ENST00000691918.1:c.233T= ENSP00000509525.1:p.Ile78=
ENST00000692152.1:c.185T= ENSP00000509317.1:p.Ile62=
ENST00000692344.1:n.278T=
ENST00000693157.1:c.174T= ENSP00000510610.1:p.Asn58=
ENST00000693363.1:c.254T= ENSP00000510411.1:p.Ile85=
ENST00000693367.1:c.254T= ENSP00000508815.1:p.Ile85=
ENST00000693639.1:c.247T= ENSP00000510223.1:p.Leu83=
ENST00000693646.1:c.160T= ENSP00000508449.1:p.Leu54=
ENST00000693716.1:n.482T=
ENST00000352397.10:c.254T= MANE Select ENSP00000338461.6:p.Ile85=
ENST00000352397.9:c.254T= ENSP00000338461.6:p.Ile85=
ENST00000361740.8:c.353T= ENSP00000354468.4:p.Ile118=
ENST00000402438.5:c.185T= ENSP00000385679.1:p.Ile62=
ENST00000407332.5:c.185T= ENSP00000384457.1:p.Ile62=
ENST00000407623.7:c.185T= ENSP00000384834.3:p.Ile62=
ENST00000438270.1:c.185T= ENSP00000403439.1:p.Ile62=
ENST00000470741.1:n.2388T=
NM_000398.6:c.254T= NP_000389.1:p.Ile85=
NM_001129819.2:c.185T= NP_001123291.1:p.Ile62=
NM_001171660.1:c.353T= NP_001165131.1:p.Ile118=
NM_001171661.1:c.185T= NP_001165132.1:p.Ile62=
NM_007326.4:c.185T= NP_015565.1:p.Ile62=
NM_000398.7:c.254T= MANE Select NP_000389.1:p.Ile85=
NM_001171660.2:c.353T= NP_001165131.1:p.Ile118=