Canonical Allele Identifier: CA411796441

Gene: CYB5R3

Linked Data

• MyVariant Identifiers: chr22:g.43019836G>C (hg19) ; chr22:g.42623830G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623830G>C , CM000684.2:g.42623830G>C	GRCh38
NC_000022.10:g.43019836G>C , CM000684.1:g.43019836G>C	GRCh37
NC_000022.9:g.41349780G>C	NCBI36
NG_012194.1:g.30570C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.824C>G	ENSP00000354468.5:p.Ala275Gly
ENST00000402438.6:c.623C>G	ENSP00000385679.1:p.Ala208Gly
ENST00000407332.6:c.710C>G	ENSP00000384457.2:p.Ala237Gly
ENST00000407623.8:c.623C>G	ENSP00000384834.3:p.Ala208Gly
ENST00000617178.5:c.229C>G
ENST00000684963.1:n.2432C>G
ENST00000685184.1:n.284C>G
ENST00000686523.1:c.*641C>G	ENSP00000508940.1:n.*641C>G
ENST00000687183.1:n.968C>G
ENST00000687198.1:c.623C>G	ENSP00000508492.1:p.Ala208Gly
ENST00000688117.1:c.791C>G	ENSP00000509015.1:p.Ala264Gly
ENST00000688244.1:c.392C>G	ENSP00000510355.1:p.Ala131Gly
ENST00000689001.1:n.1314C>G
ENST00000689195.1:c.608C>G	ENSP00000509895.1:p.Ala203Gly
ENST00000689239.1:n.859C>G
ENST00000689795.1:n.953C>G
ENST00000690835.1:c.*71C>G	ENSP00000509038.1:n.*71C>G
ENST00000690993.1:n.1447C>G
ENST00000691295.1:c.*175C>G	ENSP00000508706.1:n.*175C>G
ENST00000691918.1:c.982C>G	ENSP00000509525.1:n.982C>G
ENST00000692152.1:c.623C>G	ENSP00000509317.1:p.Ala208Gly
ENST00000692344.1:n.1179C>G
ENST00000693363.1:c.734C>G	ENSP00000510411.1:p.Ala245Gly
ENST00000693367.1:c.692C>G	ENSP00000508815.1:p.Ala231Gly
ENST00000693639.1:c.685C>G	ENSP00000510223.1:n.685C>G
ENST00000693646.1:c.598C>G	ENSP00000508449.1:n.598C>G
ENST00000352397.10:c.692C>G MANE Select	ENSP00000338461.6:p.Ala231Gly
ENST00000352397.9:c.692C>G	ENSP00000338461.6:p.Ala231Gly
ENST00000361740.8:c.791C>G	ENSP00000354468.4:p.Ala264Gly
ENST00000402438.5:c.623C>G	ENSP00000385679.1:p.Ala208Gly
ENST00000407332.5:c.623C>G	ENSP00000384457.1:p.Ala208Gly
ENST00000407623.7:c.623C>G	ENSP00000384834.3:p.Ala208Gly
ENST00000470741.1:n.2826C>G
NM_000398.6:c.692C>G	NP_000389.1:p.Ala231Gly
NM_001129819.2:c.623C>G	NP_001123291.1:p.Ala208Gly
NM_001171660.1:c.791C>G	NP_001165131.1:p.Ala264Gly
NM_001171661.1:c.623C>G	NP_001165132.1:p.Ala208Gly
NM_007326.4:c.623C>G	NP_015565.1:p.Ala208Gly
NM_000398.7:c.692C>G MANE Select	NP_000389.1:p.Ala231Gly
NM_001171660.2:c.791C>G	NP_001165131.1:p.Ala264Gly