Canonical Allele Identifier: CA411796289

Gene: CYB5R3

Linked Data

• MyVariant Identifiers: chr22:g.43019801G>T (hg19) ; chr22:g.42623795G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623795G>T , CM000684.2:g.42623795G>T	GRCh38
NC_000022.10:g.43019801G>T , CM000684.1:g.43019801G>T	GRCh37
NC_000022.9:g.41349745G>T	NCBI36
NG_012194.1:g.30605C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.859C>A	ENSP00000354468.5:p.Pro287Thr
ENST00000402438.6:c.658C>A	ENSP00000385679.1:p.Pro220Thr
ENST00000407332.6:c.745C>A	ENSP00000384457.2:p.Pro249Thr
ENST00000407623.8:c.658C>A	ENSP00000384834.3:p.Pro220Thr
ENST00000617178.5:c.264C>A
ENST00000684963.1:n.2467C>A
ENST00000685184.1:n.319C>A
ENST00000686523.1:c.*676C>A	ENSP00000508940.1:n.*676C>A
ENST00000687183.1:n.1003C>A
ENST00000687198.1:c.658C>A	ENSP00000508492.1:p.Pro220Thr
ENST00000688117.1:c.826C>A	ENSP00000509015.1:p.Pro276Thr
ENST00000688244.1:c.427C>A	ENSP00000510355.1:p.Pro143Thr
ENST00000689001.1:n.1349C>A
ENST00000689195.1:c.643C>A	ENSP00000509895.1:p.Pro215Thr
ENST00000689239.1:n.894C>A
ENST00000689795.1:n.988C>A
ENST00000690835.1:c.*106C>A	ENSP00000509038.1:n.*106C>A
ENST00000690993.1:n.1482C>A
ENST00000691295.1:c.*210C>A	ENSP00000508706.1:n.*210C>A
ENST00000691918.1:c.1017C>A	ENSP00000509525.1:n.1017C>A
ENST00000692152.1:c.658C>A	ENSP00000509317.1:p.Pro220Thr
ENST00000692344.1:n.1214C>A
ENST00000693363.1:c.769C>A	ENSP00000510411.1:p.Pro257Thr
ENST00000693367.1:c.727C>A	ENSP00000508815.1:p.Pro243Thr
ENST00000693639.1:c.720C>A	ENSP00000510223.1:n.720C>A
ENST00000693646.1:c.633C>A	ENSP00000508449.1:n.633C>A
ENST00000352397.10:c.727C>A MANE Select	ENSP00000338461.6:p.Pro243Thr
ENST00000352397.9:c.727C>A	ENSP00000338461.6:p.Pro243Thr
ENST00000361740.8:c.826C>A	ENSP00000354468.4:p.Pro276Thr
ENST00000402438.5:c.658C>A	ENSP00000385679.1:p.Pro220Thr
ENST00000407332.5:c.658C>A	ENSP00000384457.1:p.Pro220Thr
ENST00000407623.7:c.658C>A	ENSP00000384834.3:p.Pro220Thr
ENST00000470741.1:n.2861C>A
NM_000398.6:c.727C>A	NP_000389.1:p.Pro243Thr
NM_001129819.2:c.658C>A	NP_001123291.1:p.Pro220Thr
NM_001171660.1:c.826C>A	NP_001165131.1:p.Pro276Thr
NM_001171661.1:c.658C>A	NP_001165132.1:p.Pro220Thr
NM_007326.4:c.658C>A	NP_015565.1:p.Pro220Thr
NM_000398.7:c.727C>A MANE Select	NP_000389.1:p.Pro243Thr
NM_001171660.2:c.826C>A	NP_001165131.1:p.Pro276Thr