Canonical Allele Identifier: CA411796378

Gene: CYB5R3

Linked Data

• MyVariant Identifiers: chr22:g.43019822A>G (hg19) ; chr22:g.42623816A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623816A>G , CM000684.2:g.42623816A>G	GRCh38
NC_000022.10:g.43019822A>G , CM000684.1:g.43019822A>G	GRCh37
NC_000022.9:g.41349766A>G	NCBI36
NG_012194.1:g.30584T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.838T>C	ENSP00000354468.5:p.Trp280Arg
ENST00000402438.6:c.637T>C	ENSP00000385679.1:p.Trp213Arg
ENST00000407332.6:c.724T>C	ENSP00000384457.2:p.Trp242Arg
ENST00000407623.8:c.637T>C	ENSP00000384834.3:p.Trp213Arg
ENST00000617178.5:c.243T>C
ENST00000684963.1:n.2446T>C
ENST00000685184.1:n.298T>C
ENST00000686523.1:c.*655T>C	ENSP00000508940.1:n.*655T>C
ENST00000687183.1:n.982T>C
ENST00000687198.1:c.637T>C	ENSP00000508492.1:p.Trp213Arg
ENST00000688117.1:c.805T>C	ENSP00000509015.1:p.Trp269Arg
ENST00000688244.1:c.406T>C	ENSP00000510355.1:p.Trp136Arg
ENST00000689001.1:n.1328T>C
ENST00000689195.1:c.622T>C	ENSP00000509895.1:p.Trp208Arg
ENST00000689239.1:n.873T>C
ENST00000689795.1:n.967T>C
ENST00000690835.1:c.*85T>C	ENSP00000509038.1:n.*85T>C
ENST00000690993.1:n.1461T>C
ENST00000691295.1:c.*189T>C	ENSP00000508706.1:n.*189T>C
ENST00000691918.1:c.996T>C	ENSP00000509525.1:n.996T>C
ENST00000692152.1:c.637T>C	ENSP00000509317.1:p.Trp213Arg
ENST00000692344.1:n.1193T>C
ENST00000693363.1:c.748T>C	ENSP00000510411.1:p.Trp250Arg
ENST00000693367.1:c.706T>C	ENSP00000508815.1:p.Trp236Arg
ENST00000693639.1:c.699T>C	ENSP00000510223.1:n.699T>C
ENST00000693646.1:c.612T>C	ENSP00000508449.1:n.612T>C
ENST00000352397.10:c.706T>C MANE Select	ENSP00000338461.6:p.Trp236Arg
ENST00000352397.9:c.706T>C	ENSP00000338461.6:p.Trp236Arg
ENST00000361740.8:c.805T>C	ENSP00000354468.4:p.Trp269Arg
ENST00000402438.5:c.637T>C	ENSP00000385679.1:p.Trp213Arg
ENST00000407332.5:c.637T>C	ENSP00000384457.1:p.Trp213Arg
ENST00000407623.7:c.637T>C	ENSP00000384834.3:p.Trp213Arg
ENST00000470741.1:n.2840T>C
NM_000398.6:c.706T>C	NP_000389.1:p.Trp236Arg
NM_001129819.2:c.637T>C	NP_001123291.1:p.Trp213Arg
NM_001171660.1:c.805T>C	NP_001165131.1:p.Trp269Arg
NM_001171661.1:c.637T>C	NP_001165132.1:p.Trp213Arg
NM_007326.4:c.637T>C	NP_015565.1:p.Trp213Arg
NM_000398.7:c.706T>C MANE Select	NP_000389.1:p.Trp236Arg
NM_001171660.2:c.805T>C	NP_001165131.1:p.Trp269Arg