Canonical Allele Identifier: CA2406839062

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42630915A= , CM000684.2:g.42630915A=	GRCh38
NC_000022.10:g.43026921A= , CM000684.1:g.43026921A=	GRCh37
NC_000022.9:g.41356865A=	NCBI36
NG_012194.1:g.23485T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.300T=	ENSP00000354468.5:p.Asp100=
ENST00000402438.6:c.231T=	ENSP00000385679.1:p.Asp77=
ENST00000407332.6:c.318T=	ENSP00000384457.2:p.Asp106=
ENST00000407623.8:c.231T=	ENSP00000384834.3:p.Asp77=
ENST00000438270.2:c.231T=	ENSP00000403439.2:p.Asp77=
ENST00000466276.2:n.367T=
ENST00000686129.1:c.231T=	ENSP00000508623.1:p.Asp77=
ENST00000686523.1:c.*249T=	ENSP00000508940.1:n.*249T=
ENST00000687183.1:n.361T=
ENST00000687198.1:c.231T=	ENSP00000508492.1:p.Asp77=
ENST00000688117.1:c.399T=	ENSP00000509015.1:p.Asp133=
ENST00000688244.1:c.300T=	ENSP00000510355.1:p.Asp100=
ENST00000689001.1:n.707T=
ENST00000689195.1:c.300T=	ENSP00000509895.1:p.Asp100=
ENST00000689239.1:n.467T=
ENST00000689795.1:n.462T=
ENST00000690835.1:c.300T=	ENSP00000509038.1:p.Asp100=
ENST00000690993.1:n.377T=
ENST00000691295.1:c.300T=	ENSP00000508706.1:p.Asp100=
ENST00000691918.1:c.279T=	ENSP00000509525.1:p.Asp93=
ENST00000692152.1:c.231T=	ENSP00000509317.1:p.Asp77=
ENST00000692344.1:n.324T=
ENST00000693157.1:c.220T=	ENSP00000510610.1:n.220T=
ENST00000693363.1:c.300T=	ENSP00000510411.1:p.Asp100=
ENST00000693367.1:c.300T=	ENSP00000508815.1:p.Asp100=
ENST00000693639.1:c.293T=	ENSP00000510223.1:p.Met98=
ENST00000693646.1:c.206T=	ENSP00000508449.1:p.Met69=
ENST00000693716.1:n.528T=
ENST00000352397.10:c.300T= MANE Select	ENSP00000338461.6:p.Asp100=
ENST00000352397.9:c.300T=	ENSP00000338461.6:p.Asp100=
ENST00000361740.8:c.399T=	ENSP00000354468.4:p.Asp133=
ENST00000402438.5:c.231T=	ENSP00000385679.1:p.Asp77=
ENST00000407332.5:c.231T=	ENSP00000384457.1:p.Asp77=
ENST00000407623.7:c.231T=	ENSP00000384834.3:p.Asp77=
ENST00000438270.1:c.231T=	ENSP00000403439.1:p.Asp77=
ENST00000470741.1:n.2434T=
NM_000398.6:c.300T=	NP_000389.1:p.Asp100=
NM_001129819.2:c.231T=	NP_001123291.1:p.Asp77=
NM_001171660.1:c.399T=	NP_001165131.1:p.Asp133=
NM_001171661.1:c.231T=	NP_001165132.1:p.Asp77=
NM_007326.4:c.231T=	NP_015565.1:p.Asp77=
NM_000398.7:c.300T= MANE Select	NP_000389.1:p.Asp100=
NM_001171660.2:c.399T=	NP_001165131.1:p.Asp133=