Canonical Allele Identifier: CA514816103

Gene: CYB5R3

Linked Data

• COSMIC: COSM726937 ; COSM1149488
• MyVariant Identifiers: chr22:g.43024195G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42628189G>A , CM000684.2:g.42628189G>A	GRCh38
NC_000022.10:g.43024195G>A , CM000684.1:g.43024195G>A	GRCh37
NC_000022.9:g.41354139G>A	NCBI36
NG_012194.1:g.26211C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.426C>T	ENSP00000354468.5:p.Phe142=
ENST00000402438.6:c.357C>T	ENSP00000385679.1:p.Phe119=
ENST00000407332.6:c.444C>T	ENSP00000384457.2:p.Phe148=
ENST00000407623.8:c.357C>T	ENSP00000384834.3:p.Phe119=
ENST00000438270.2:c.357C>T	ENSP00000403439.2:p.Phe119=
ENST00000684963.1:n.1703C>T
ENST00000686129.1:c.357C>T	ENSP00000508623.1:p.Phe119=
ENST00000686523.1:c.*375C>T	ENSP00000508940.1:n.*375C>T
ENST00000687183.1:n.487C>T
ENST00000687198.1:c.357C>T	ENSP00000508492.1:p.Phe119=
ENST00000688117.1:c.525C>T	ENSP00000509015.1:p.Phe175=
ENST00000688244.1:c.333+2693C>T	ENSP00000510355.1:n.333+2693C>T
ENST00000689001.1:n.833C>T
ENST00000689195.1:c.426C>T	ENSP00000509895.1:p.Phe142=
ENST00000689239.1:n.593C>T
ENST00000689795.1:n.588C>T
ENST00000690835.1:c.426C>T	ENSP00000509038.1:p.Phe142=
ENST00000690993.1:n.503C>T
ENST00000691295.1:c.334-501C>T	ENSP00000508706.1:n.334-501C>T
ENST00000691918.1:c.405C>T	ENSP00000509525.1:p.Phe135=
ENST00000692152.1:c.357C>T	ENSP00000509317.1:p.Phe119=
ENST00000692344.1:n.450C>T
ENST00000693157.1:c.346C>T	ENSP00000510610.1:n.346C>T
ENST00000693363.1:c.426C>T	ENSP00000510411.1:p.Phe142=
ENST00000693367.1:c.426C>T	ENSP00000508815.1:p.Phe142=
ENST00000693639.1:c.419C>T	ENSP00000510223.1:p.Ser140Phe
ENST00000693646.1:c.332C>T	ENSP00000508449.1:p.Ser111Phe
ENST00000352397.10:c.426C>T MANE Select	ENSP00000338461.6:p.Phe142=
ENST00000352397.9:c.426C>T	ENSP00000338461.6:p.Phe142=
ENST00000361740.8:c.525C>T	ENSP00000354468.4:p.Phe175=
ENST00000402438.5:c.357C>T	ENSP00000385679.1:p.Phe119=
ENST00000407332.5:c.357C>T	ENSP00000384457.1:p.Phe119=
ENST00000407623.7:c.357C>T	ENSP00000384834.3:p.Phe119=
ENST00000438270.1:c.357C>T	ENSP00000403439.1:p.Phe119=
ENST00000470741.1:n.2560C>T
NM_000398.6:c.426C>T	NP_000389.1:p.Phe142=
NM_001129819.2:c.357C>T	NP_001123291.1:p.Phe119=
NM_001171660.1:c.525C>T	NP_001165131.1:p.Phe175=
NM_001171661.1:c.357C>T	NP_001165132.1:p.Phe119=
NM_007326.4:c.357C>T	NP_015565.1:p.Phe119=
NM_000398.7:c.426C>T MANE Select	NP_000389.1:p.Phe142=
NM_001171660.2:c.525C>T	NP_001165131.1:p.Phe175=