Canonical Allele Identifier: CA411799737

Gene: CYB5R3

Linked Data

• MyVariant Identifiers: chr22:g.43024283T>C (hg19) ; chr22:g.42628277T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42628277T>C , CM000684.2:g.42628277T>C	GRCh38
NC_000022.10:g.43024283T>C , CM000684.1:g.43024283T>C	GRCh37
NC_000022.9:g.41354227T>C	NCBI36
NG_012194.1:g.26123A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.338A>G	ENSP00000354468.5:p.Tyr113Cys
ENST00000402438.6:c.269A>G	ENSP00000385679.1:p.Tyr90Cys
ENST00000407332.6:c.356A>G	ENSP00000384457.2:p.Tyr119Cys
ENST00000407623.8:c.269A>G	ENSP00000384834.3:p.Tyr90Cys
ENST00000438270.2:c.269A>G	ENSP00000403439.2:p.Tyr90Cys
ENST00000684963.1:n.1615A>G
ENST00000686129.1:c.269A>G	ENSP00000508623.1:p.Tyr90Cys
ENST00000686523.1:c.*287A>G	ENSP00000508940.1:n.*287A>G
ENST00000687183.1:n.399A>G
ENST00000687198.1:c.269A>G	ENSP00000508492.1:p.Tyr90Cys
ENST00000688117.1:c.437A>G	ENSP00000509015.1:p.Tyr146Cys
ENST00000688244.1:c.333+2605A>G	ENSP00000510355.1:n.333+2605A>G
ENST00000689001.1:n.745A>G
ENST00000689195.1:c.338A>G	ENSP00000509895.1:p.Tyr113Cys
ENST00000689239.1:n.505A>G
ENST00000689795.1:n.500A>G
ENST00000690835.1:c.338A>G	ENSP00000509038.1:p.Tyr113Cys
ENST00000690993.1:n.415A>G
ENST00000691295.1:c.334-589A>G	ENSP00000508706.1:n.334-589A>G
ENST00000691918.1:c.317A>G	ENSP00000509525.1:p.Tyr106Cys
ENST00000692152.1:c.269A>G	ENSP00000509317.1:p.Tyr90Cys
ENST00000692344.1:n.362A>G
ENST00000693157.1:c.258A>G	ENSP00000510610.1:n.258A>G
ENST00000693363.1:c.338A>G	ENSP00000510411.1:p.Tyr113Cys
ENST00000693367.1:c.338A>G	ENSP00000508815.1:p.Tyr113Cys
ENST00000693639.1:c.331A>G	ENSP00000510223.1:p.Thr111Ala
ENST00000693646.1:c.244A>G	ENSP00000508449.1:p.Thr82Ala
ENST00000352397.10:c.338A>G MANE Select	ENSP00000338461.6:p.Tyr113Cys
ENST00000352397.9:c.338A>G	ENSP00000338461.6:p.Tyr113Cys
ENST00000361740.8:c.437A>G	ENSP00000354468.4:p.Tyr146Cys
ENST00000402438.5:c.269A>G	ENSP00000385679.1:p.Tyr90Cys
ENST00000407332.5:c.269A>G	ENSP00000384457.1:p.Tyr90Cys
ENST00000407623.7:c.269A>G	ENSP00000384834.3:p.Tyr90Cys
ENST00000438270.1:c.269A>G	ENSP00000403439.1:p.Tyr90Cys
ENST00000470741.1:n.2472A>G
NM_000398.6:c.338A>G	NP_000389.1:p.Tyr113Cys
NM_001129819.2:c.269A>G	NP_001123291.1:p.Tyr90Cys
NM_001171660.1:c.437A>G	NP_001165131.1:p.Tyr146Cys
NM_001171661.1:c.269A>G	NP_001165132.1:p.Tyr90Cys
NM_007326.4:c.269A>G	NP_015565.1:p.Tyr90Cys
NM_000398.7:c.338A>G MANE Select	NP_000389.1:p.Tyr113Cys
NM_001171660.2:c.437A>G	NP_001165131.1:p.Tyr146Cys