Canonical Allele Identifier: CA411796399

Gene: CYB5R3

Linked Data

• MyVariant Identifiers: chr22:g.43019827T>C (hg19) ; chr22:g.42623821T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623821T>C , CM000684.2:g.42623821T>C	GRCh38
NC_000022.10:g.43019827T>C , CM000684.1:g.43019827T>C	GRCh37
NC_000022.9:g.41349771T>C	NCBI36
NG_012194.1:g.30579A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.833A>G	ENSP00000354468.5:p.Lys278Arg
ENST00000402438.6:c.632A>G	ENSP00000385679.1:p.Lys211Arg
ENST00000407332.6:c.719A>G	ENSP00000384457.2:p.Lys240Arg
ENST00000407623.8:c.632A>G	ENSP00000384834.3:p.Lys211Arg
ENST00000617178.5:c.238A>G
ENST00000684963.1:n.2441A>G
ENST00000685184.1:n.293A>G
ENST00000686523.1:c.*650A>G	ENSP00000508940.1:n.*650A>G
ENST00000687183.1:n.977A>G
ENST00000687198.1:c.632A>G	ENSP00000508492.1:p.Lys211Arg
ENST00000688117.1:c.800A>G	ENSP00000509015.1:p.Lys267Arg
ENST00000688244.1:c.401A>G	ENSP00000510355.1:p.Lys134Arg
ENST00000689001.1:n.1323A>G
ENST00000689195.1:c.617A>G	ENSP00000509895.1:p.Lys206Arg
ENST00000689239.1:n.868A>G
ENST00000689795.1:n.962A>G
ENST00000690835.1:c.*80A>G	ENSP00000509038.1:n.*80A>G
ENST00000690993.1:n.1456A>G
ENST00000691295.1:c.*184A>G	ENSP00000508706.1:n.*184A>G
ENST00000691918.1:c.991A>G	ENSP00000509525.1:n.991A>G
ENST00000692152.1:c.632A>G	ENSP00000509317.1:p.Lys211Arg
ENST00000692344.1:n.1188A>G
ENST00000693363.1:c.743A>G	ENSP00000510411.1:p.Lys248Arg
ENST00000693367.1:c.701A>G	ENSP00000508815.1:p.Lys234Arg
ENST00000693639.1:c.694A>G	ENSP00000510223.1:n.694A>G
ENST00000693646.1:c.607A>G	ENSP00000508449.1:n.607A>G
ENST00000352397.10:c.701A>G MANE Select	ENSP00000338461.6:p.Lys234Arg
ENST00000352397.9:c.701A>G	ENSP00000338461.6:p.Lys234Arg
ENST00000361740.8:c.800A>G	ENSP00000354468.4:p.Lys267Arg
ENST00000402438.5:c.632A>G	ENSP00000385679.1:p.Lys211Arg
ENST00000407332.5:c.632A>G	ENSP00000384457.1:p.Lys211Arg
ENST00000407623.7:c.632A>G	ENSP00000384834.3:p.Lys211Arg
ENST00000470741.1:n.2835A>G
NM_000398.6:c.701A>G	NP_000389.1:p.Lys234Arg
NM_001129819.2:c.632A>G	NP_001123291.1:p.Lys211Arg
NM_001171660.1:c.800A>G	NP_001165131.1:p.Lys267Arg
NM_001171661.1:c.632A>G	NP_001165132.1:p.Lys211Arg
NM_007326.4:c.632A>G	NP_015565.1:p.Lys211Arg
NM_000398.7:c.701A>G MANE Select	NP_000389.1:p.Lys234Arg
NM_001171660.2:c.800A>G	NP_001165131.1:p.Lys267Arg