Canonical Allele Identifier: CA411796283

Gene: CYB5R3

Linked Data

• MyVariant Identifiers: chr22:g.43019800G>C (hg19) ; chr22:g.42623794G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623794G>C , CM000684.2:g.42623794G>C	GRCh38
NC_000022.10:g.43019800G>C , CM000684.1:g.43019800G>C	GRCh37
NC_000022.9:g.41349744G>C	NCBI36
NG_012194.1:g.30606C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361740.9:c.860C>G	ENSP00000354468.5:p.Pro287Arg
ENST00000402438.6:c.659C>G	ENSP00000385679.1:p.Pro220Arg
ENST00000407332.6:c.746C>G	ENSP00000384457.2:p.Pro249Arg
ENST00000407623.8:c.659C>G	ENSP00000384834.3:p.Pro220Arg
ENST00000617178.5:c.265C>G
ENST00000684963.1:n.2468C>G
ENST00000685184.1:n.320C>G
ENST00000686523.1:c.*677C>G	ENSP00000508940.1:n.*677C>G
ENST00000687183.1:n.1004C>G
ENST00000687198.1:c.659C>G	ENSP00000508492.1:p.Pro220Arg
ENST00000688117.1:c.827C>G	ENSP00000509015.1:p.Pro276Arg
ENST00000688244.1:c.428C>G	ENSP00000510355.1:p.Pro143Arg
ENST00000689001.1:n.1350C>G
ENST00000689195.1:c.644C>G	ENSP00000509895.1:p.Pro215Arg
ENST00000689239.1:n.895C>G
ENST00000689795.1:n.989C>G
ENST00000690835.1:c.*107C>G	ENSP00000509038.1:n.*107C>G
ENST00000690993.1:n.1483C>G
ENST00000691295.1:c.*211C>G	ENSP00000508706.1:n.*211C>G
ENST00000691918.1:c.1018C>G	ENSP00000509525.1:n.1018C>G
ENST00000692152.1:c.659C>G	ENSP00000509317.1:p.Pro220Arg
ENST00000692344.1:n.1215C>G
ENST00000693363.1:c.770C>G	ENSP00000510411.1:p.Pro257Arg
ENST00000693367.1:c.728C>G	ENSP00000508815.1:p.Pro243Arg
ENST00000693639.1:c.721C>G	ENSP00000510223.1:n.721C>G
ENST00000693646.1:c.634C>G	ENSP00000508449.1:n.634C>G
ENST00000352397.10:c.728C>G MANE Select	ENSP00000338461.6:p.Pro243Arg
ENST00000352397.9:c.728C>G	ENSP00000338461.6:p.Pro243Arg
ENST00000361740.8:c.827C>G	ENSP00000354468.4:p.Pro276Arg
ENST00000402438.5:c.659C>G	ENSP00000385679.1:p.Pro220Arg
ENST00000407332.5:c.659C>G	ENSP00000384457.1:p.Pro220Arg
ENST00000407623.7:c.659C>G	ENSP00000384834.3:p.Pro220Arg
ENST00000470741.1:n.2862C>G
NM_000398.6:c.728C>G	NP_000389.1:p.Pro243Arg
NM_001129819.2:c.659C>G	NP_001123291.1:p.Pro220Arg
NM_001171660.1:c.827C>G	NP_001165131.1:p.Pro276Arg
NM_001171661.1:c.659C>G	NP_001165132.1:p.Pro220Arg
NM_007326.4:c.659C>G	NP_015565.1:p.Pro220Arg
NM_000398.7:c.728C>G MANE Select	NP_000389.1:p.Pro243Arg
NM_001171660.2:c.827C>G	NP_001165131.1:p.Pro276Arg