Canonical Allele Identifier: CA411796646

Gene: CYB5R3

Linked Data

• MyVariant Identifiers: chr22:g.43019869G>C (hg19) ; chr22:g.42623863G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623863G>C , CM000684.2:g.42623863G>C	GRCh38
NC_000022.10:g.43019869G>C , CM000684.1:g.43019869G>C	GRCh37
NC_000022.9:g.41349813G>C	NCBI36
NG_012194.1:g.30537C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.791C>G	ENSP00000354468.5:p.Pro264Arg
ENST00000402438.6:c.590C>G	ENSP00000385679.1:p.Pro197Arg
ENST00000407332.6:c.677C>G	ENSP00000384457.2:p.Pro226Arg
ENST00000407623.8:c.590C>G	ENSP00000384834.3:p.Pro197Arg
ENST00000617178.5:c.196C>G
ENST00000684963.1:n.2399C>G
ENST00000685184.1:n.251C>G
ENST00000686523.1:c.*608C>G	ENSP00000508940.1:n.*608C>G
ENST00000687183.1:n.935C>G
ENST00000687198.1:c.590C>G	ENSP00000508492.1:p.Pro197Arg
ENST00000688117.1:c.758C>G	ENSP00000509015.1:p.Pro253Arg
ENST00000688244.1:c.359C>G	ENSP00000510355.1:p.Pro120Arg
ENST00000689001.1:n.1281C>G
ENST00000689195.1:c.575C>G	ENSP00000509895.1:p.Pro192Arg
ENST00000689239.1:n.826C>G
ENST00000689795.1:n.920C>G
ENST00000690835.1:c.*38C>G	ENSP00000509038.1:n.*38C>G
ENST00000690993.1:n.1414C>G
ENST00000691295.1:c.*142C>G	ENSP00000508706.1:n.*142C>G
ENST00000691918.1:c.949C>G	ENSP00000509525.1:n.949C>G
ENST00000692152.1:c.590C>G	ENSP00000509317.1:p.Pro197Arg
ENST00000692344.1:n.1146C>G
ENST00000693363.1:c.701C>G	ENSP00000510411.1:p.Pro234Arg
ENST00000693367.1:c.659C>G	ENSP00000508815.1:p.Pro220Arg
ENST00000693639.1:c.652C>G	ENSP00000510223.1:n.652C>G
ENST00000693646.1:c.565C>G	ENSP00000508449.1:n.565C>G
ENST00000352397.10:c.659C>G MANE Select	ENSP00000338461.6:p.Pro220Arg
ENST00000352397.9:c.659C>G	ENSP00000338461.6:p.Pro220Arg
ENST00000361740.8:c.758C>G	ENSP00000354468.4:p.Pro253Arg
ENST00000402438.5:c.590C>G	ENSP00000385679.1:p.Pro197Arg
ENST00000407332.5:c.590C>G	ENSP00000384457.1:p.Pro197Arg
ENST00000407623.7:c.590C>G	ENSP00000384834.3:p.Pro197Arg
ENST00000470741.1:n.2793C>G
NM_000398.6:c.659C>G	NP_000389.1:p.Pro220Arg
NM_001129819.2:c.590C>G	NP_001123291.1:p.Pro197Arg
NM_001171660.1:c.758C>G	NP_001165131.1:p.Pro253Arg
NM_001171661.1:c.590C>G	NP_001165132.1:p.Pro197Arg
NM_007326.4:c.590C>G	NP_015565.1:p.Pro197Arg
NM_000398.7:c.659C>G MANE Select	NP_000389.1:p.Pro220Arg
NM_001171660.2:c.758C>G	NP_001165131.1:p.Pro253Arg