Canonical Allele Identifier: CA411799253

Gene: CYB5R3

Linked Data

• MyVariant Identifiers: chr22:g.43024208T>G (hg19) ; chr22:g.42628202T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42628202T>G , CM000684.2:g.42628202T>G	GRCh38
NC_000022.10:g.43024208T>G , CM000684.1:g.43024208T>G	GRCh37
NC_000022.9:g.41354152T>G	NCBI36
NG_012194.1:g.26198A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.413A>C	ENSP00000354468.5:p.Asp138Ala
ENST00000402438.6:c.344A>C	ENSP00000385679.1:p.Asp115Ala
ENST00000407332.6:c.431A>C	ENSP00000384457.2:p.Asp144Ala
ENST00000407623.8:c.344A>C	ENSP00000384834.3:p.Asp115Ala
ENST00000438270.2:c.344A>C	ENSP00000403439.2:p.Asp115Ala
ENST00000684963.1:n.1690A>C
ENST00000686129.1:c.344A>C	ENSP00000508623.1:p.Asp115Ala
ENST00000686523.1:c.*362A>C	ENSP00000508940.1:n.*362A>C
ENST00000687183.1:n.474A>C
ENST00000687198.1:c.344A>C	ENSP00000508492.1:p.Asp115Ala
ENST00000688117.1:c.512A>C	ENSP00000509015.1:p.Asp171Ala
ENST00000688244.1:c.333+2680A>C	ENSP00000510355.1:n.333+2680A>C
ENST00000689001.1:n.820A>C
ENST00000689195.1:c.413A>C	ENSP00000509895.1:p.Asp138Ala
ENST00000689239.1:n.580A>C
ENST00000689795.1:n.575A>C
ENST00000690835.1:c.413A>C	ENSP00000509038.1:p.Asp138Ala
ENST00000690993.1:n.490A>C
ENST00000691295.1:c.334-514A>C	ENSP00000508706.1:n.334-514A>C
ENST00000691918.1:c.392A>C	ENSP00000509525.1:p.Asp131Ala
ENST00000692152.1:c.344A>C	ENSP00000509317.1:p.Asp115Ala
ENST00000692344.1:n.437A>C
ENST00000693157.1:c.333A>C	ENSP00000510610.1:n.333A>C
ENST00000693363.1:c.413A>C	ENSP00000510411.1:p.Asp138Ala
ENST00000693367.1:c.413A>C	ENSP00000508815.1:p.Asp138Ala
ENST00000693639.1:c.406A>C	ENSP00000510223.1:p.Thr136Pro
ENST00000693646.1:c.319A>C	ENSP00000508449.1:p.Thr107Pro
ENST00000352397.10:c.413A>C MANE Select	ENSP00000338461.6:p.Asp138Ala
ENST00000352397.9:c.413A>C	ENSP00000338461.6:p.Asp138Ala
ENST00000361740.8:c.512A>C	ENSP00000354468.4:p.Asp171Ala
ENST00000402438.5:c.344A>C	ENSP00000385679.1:p.Asp115Ala
ENST00000407332.5:c.344A>C	ENSP00000384457.1:p.Asp115Ala
ENST00000407623.7:c.344A>C	ENSP00000384834.3:p.Asp115Ala
ENST00000438270.1:c.344A>C	ENSP00000403439.1:p.Asp115Ala
ENST00000470741.1:n.2547A>C
NM_000398.6:c.413A>C	NP_000389.1:p.Asp138Ala
NM_001129819.2:c.344A>C	NP_001123291.1:p.Asp115Ala
NM_001171660.1:c.512A>C	NP_001165131.1:p.Asp171Ala
NM_001171661.1:c.344A>C	NP_001165132.1:p.Asp115Ala
NM_007326.4:c.344A>C	NP_015565.1:p.Asp115Ala
NM_000398.7:c.413A>C MANE Select	NP_000389.1:p.Asp138Ala
NM_001171660.2:c.512A>C	NP_001165131.1:p.Asp171Ala