Canonical Allele Identifier: CA2406837558
Gene: CYB5R3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42628222C= , CM000684.2:g.42628222C= GRCh38
NC_000022.10:g.43024228C= , CM000684.1:g.43024228C= GRCh37
NC_000022.9:g.41354172C= NCBI36
NG_012194.1:g.26178G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.393G= ENSP00000354468.5:p.Leu131=
ENST00000402438.6:c.324G= ENSP00000385679.1:p.Leu108=
ENST00000407332.6:c.411G= ENSP00000384457.2:p.Leu137=
ENST00000407623.8:c.324G= ENSP00000384834.3:p.Leu108=
ENST00000438270.2:c.324G= ENSP00000403439.2:p.Leu108=
ENST00000684963.1:n.1670G=
ENST00000686129.1:c.324G= ENSP00000508623.1:p.Leu108=
ENST00000686523.1:c.*342G= ENSP00000508940.1:n.*342G=
ENST00000687183.1:n.454G=
ENST00000687198.1:c.324G= ENSP00000508492.1:p.Leu108=
ENST00000688117.1:c.492G= ENSP00000509015.1:p.Leu164=
ENST00000688244.1:c.333+2660G= ENSP00000510355.1:n.333+2660G=
ENST00000689001.1:n.800G=
ENST00000689195.1:c.393G= ENSP00000509895.1:p.Leu131=
ENST00000689239.1:n.560G=
ENST00000689795.1:n.555G=
ENST00000690835.1:c.393G= ENSP00000509038.1:p.Leu131=
ENST00000690993.1:n.470G=
ENST00000691295.1:c.334-534G= ENSP00000508706.1:n.334-534G=
ENST00000691918.1:c.372G= ENSP00000509525.1:p.Leu124=
ENST00000692152.1:c.324G= ENSP00000509317.1:p.Leu108=
ENST00000692344.1:n.417G=
ENST00000693157.1:c.313G= ENSP00000510610.1:n.313G=
ENST00000693363.1:c.393G= ENSP00000510411.1:p.Leu131=
ENST00000693367.1:c.393G= ENSP00000508815.1:p.Leu131=
ENST00000693639.1:c.386G= ENSP00000510223.1:p.Trp129=
ENST00000693646.1:c.299G= ENSP00000508449.1:p.Trp100=
ENST00000352397.10:c.393G= MANE Select ENSP00000338461.6:p.Leu131=
ENST00000352397.9:c.393G= ENSP00000338461.6:p.Leu131=
ENST00000361740.8:c.492G= ENSP00000354468.4:p.Leu164=
ENST00000402438.5:c.324G= ENSP00000385679.1:p.Leu108=
ENST00000407332.5:c.324G= ENSP00000384457.1:p.Leu108=
ENST00000407623.7:c.324G= ENSP00000384834.3:p.Leu108=
ENST00000438270.1:c.324G= ENSP00000403439.1:p.Leu108=
ENST00000470741.1:n.2527G=
NM_000398.6:c.393G= NP_000389.1:p.Leu131=
NM_001129819.2:c.324G= NP_001123291.1:p.Leu108=
NM_001171660.1:c.492G= NP_001165131.1:p.Leu164=
NM_001171661.1:c.324G= NP_001165132.1:p.Leu108=
NM_007326.4:c.324G= NP_015565.1:p.Leu108=
NM_000398.7:c.393G= MANE Select NP_000389.1:p.Leu131=
NM_001171660.2:c.492G= NP_001165131.1:p.Leu164=