Canonical Allele Identifier: CA411796787

Gene: CYB5R3

Linked Data

• MyVariant Identifiers: chr22:g.43019894T>A (hg19) ; chr22:g.42623888T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623888T>A , CM000684.2:g.42623888T>A	GRCh38
NC_000022.10:g.43019894T>A , CM000684.1:g.43019894T>A	GRCh37
NC_000022.9:g.41349838T>A	NCBI36
NG_012194.1:g.30512A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.766A>T	ENSP00000354468.5:p.Thr256Ser
ENST00000402438.6:c.565A>T	ENSP00000385679.1:p.Thr189Ser
ENST00000407332.6:c.652A>T	ENSP00000384457.2:p.Thr218Ser
ENST00000407623.8:c.565A>T	ENSP00000384834.3:p.Thr189Ser
ENST00000617178.5:c.171A>T
ENST00000684963.1:n.2374A>T
ENST00000685184.1:n.226A>T
ENST00000686523.1:c.*583A>T	ENSP00000508940.1:n.*583A>T
ENST00000687183.1:n.910A>T
ENST00000687198.1:c.565A>T	ENSP00000508492.1:p.Thr189Ser
ENST00000688117.1:c.733A>T	ENSP00000509015.1:p.Thr245Ser
ENST00000688244.1:c.334A>T	ENSP00000510355.1:p.Thr112Ser
ENST00000689001.1:n.1256A>T
ENST00000689195.1:c.550A>T	ENSP00000509895.1:p.Thr184Ser
ENST00000689239.1:n.801A>T
ENST00000689795.1:n.895A>T
ENST00000690835.1:c.*13A>T	ENSP00000509038.1:n.*13A>T
ENST00000690993.1:n.1389A>T
ENST00000691295.1:c.*117A>T	ENSP00000508706.1:n.*117A>T
ENST00000691918.1:c.924A>T	ENSP00000509525.1:n.924A>T
ENST00000692152.1:c.565A>T	ENSP00000509317.1:p.Thr189Ser
ENST00000692344.1:n.1121A>T
ENST00000693363.1:c.676A>T	ENSP00000510411.1:p.Thr226Ser
ENST00000693367.1:c.634A>T	ENSP00000508815.1:p.Thr212Ser
ENST00000693639.1:c.627A>T	ENSP00000510223.1:n.627A>T
ENST00000693646.1:c.540A>T	ENSP00000508449.1:n.540A>T
ENST00000352397.10:c.634A>T MANE Select	ENSP00000338461.6:p.Thr212Ser
ENST00000352397.9:c.634A>T	ENSP00000338461.6:p.Thr212Ser
ENST00000361740.8:c.733A>T	ENSP00000354468.4:p.Thr245Ser
ENST00000402438.5:c.565A>T	ENSP00000385679.1:p.Thr189Ser
ENST00000407332.5:c.565A>T	ENSP00000384457.1:p.Thr189Ser
ENST00000407623.7:c.565A>T	ENSP00000384834.3:p.Thr189Ser
ENST00000470741.1:n.2768A>T
NM_000398.6:c.634A>T	NP_000389.1:p.Thr212Ser
NM_001129819.2:c.565A>T	NP_001123291.1:p.Thr189Ser
NM_001171660.1:c.733A>T	NP_001165131.1:p.Thr245Ser
NM_001171661.1:c.565A>T	NP_001165132.1:p.Thr189Ser
NM_007326.4:c.565A>T	NP_015565.1:p.Thr189Ser
NM_000398.7:c.634A>T MANE Select	NP_000389.1:p.Thr212Ser
NM_001171660.2:c.733A>T	NP_001165131.1:p.Thr245Ser