Canonical Allele Identifier: CA411799462
Gene: CYB5R3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42628233A>C , CM000684.2:g.42628233A>C GRCh38
NC_000022.10:g.43024239A>C , CM000684.1:g.43024239A>C GRCh37
NC_000022.9:g.41354183A>C NCBI36
NG_012194.1:g.26167T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.382T>G ENSP00000354468.5:p.Ser128Ala
ENST00000402438.6:c.313T>G ENSP00000385679.1:p.Ser105Ala
ENST00000407332.6:c.400T>G ENSP00000384457.2:p.Ser134Ala
ENST00000407623.8:c.313T>G ENSP00000384834.3:p.Ser105Ala
ENST00000438270.2:c.313T>G ENSP00000403439.2:p.Ser105Ala
ENST00000684963.1:n.1659T>G
ENST00000686129.1:c.313T>G ENSP00000508623.1:p.Ser105Ala
ENST00000686523.1:c.*331T>G ENSP00000508940.1:n.*331T>G
ENST00000687183.1:n.443T>G
ENST00000687198.1:c.313T>G ENSP00000508492.1:p.Ser105Ala
ENST00000688117.1:c.481T>G ENSP00000509015.1:p.Ser161Ala
ENST00000688244.1:c.333+2649T>G ENSP00000510355.1:n.333+2649T>G
ENST00000689001.1:n.789T>G
ENST00000689195.1:c.382T>G ENSP00000509895.1:p.Ser128Ala
ENST00000689239.1:n.549T>G
ENST00000689795.1:n.544T>G
ENST00000690835.1:c.382T>G ENSP00000509038.1:p.Ser128Ala
ENST00000690993.1:n.459T>G
ENST00000691295.1:c.334-545T>G ENSP00000508706.1:n.334-545T>G
ENST00000691918.1:c.361T>G ENSP00000509525.1:p.Ser121Ala
ENST00000692152.1:c.313T>G ENSP00000509317.1:p.Ser105Ala
ENST00000692344.1:n.406T>G
ENST00000693157.1:c.302T>G ENSP00000510610.1:n.302T>G
ENST00000693363.1:c.382T>G ENSP00000510411.1:p.Ser128Ala
ENST00000693367.1:c.382T>G ENSP00000508815.1:p.Ser128Ala
ENST00000693639.1:c.375T>G ENSP00000510223.1:p.Cys125Trp
ENST00000693646.1:c.288T>G ENSP00000508449.1:p.Cys96Trp
ENST00000352397.10:c.382T>G MANE Select ENSP00000338461.6:p.Ser128Ala
ENST00000352397.9:c.382T>G ENSP00000338461.6:p.Ser128Ala
ENST00000361740.8:c.481T>G ENSP00000354468.4:p.Ser161Ala
ENST00000402438.5:c.313T>G ENSP00000385679.1:p.Ser105Ala
ENST00000407332.5:c.313T>G ENSP00000384457.1:p.Ser105Ala
ENST00000407623.7:c.313T>G ENSP00000384834.3:p.Ser105Ala
ENST00000438270.1:c.313T>G ENSP00000403439.1:p.Ser105Ala
ENST00000470741.1:n.2516T>G
NM_000398.6:c.382T>G NP_000389.1:p.Ser128Ala
NM_001129819.2:c.313T>G NP_001123291.1:p.Ser105Ala
NM_001171660.1:c.481T>G NP_001165131.1:p.Ser161Ala
NM_001171661.1:c.313T>G NP_001165132.1:p.Ser105Ala
NM_007326.4:c.313T>G NP_015565.1:p.Ser105Ala
NM_000398.7:c.382T>G MANE Select NP_000389.1:p.Ser128Ala
NM_001171660.2:c.481T>G NP_001165131.1:p.Ser161Ala