Canonical Allele Identifier: CA514816019

Gene: CYB5R3

Linked Data

• dbSNP Id: rs2146877726
• MyVariant Identifiers: chr22:g.43024183A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42628177A>G , CM000684.2:g.42628177A>G	GRCh38
NC_000022.10:g.43024183A>G , CM000684.1:g.43024183A>G	GRCh37
NC_000022.9:g.41354127A>G	NCBI36
NG_012194.1:g.26223T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.438T>C	ENSP00000354468.5:p.Ser146=
ENST00000402438.6:c.369T>C	ENSP00000385679.1:p.Ser123=
ENST00000407332.6:c.456T>C	ENSP00000384457.2:p.Ser152=
ENST00000407623.8:c.369T>C	ENSP00000384834.3:p.Ser123=
ENST00000438270.2:c.369T>C	ENSP00000403439.2:p.Ser123=
ENST00000684963.1:n.1715T>C
ENST00000686129.1:c.369T>C	ENSP00000508623.1:p.Ser123=
ENST00000686523.1:c.*387T>C	ENSP00000508940.1:n.*387T>C
ENST00000687183.1:n.499T>C
ENST00000687198.1:c.369T>C	ENSP00000508492.1:p.Ser123=
ENST00000688117.1:c.537T>C	ENSP00000509015.1:p.Ser179=
ENST00000688244.1:c.333+2705T>C	ENSP00000510355.1:n.333+2705T>C
ENST00000689001.1:n.845T>C
ENST00000689195.1:c.438T>C	ENSP00000509895.1:p.Ser146=
ENST00000689239.1:n.605T>C
ENST00000689795.1:n.600T>C
ENST00000690835.1:c.438T>C	ENSP00000509038.1:p.Ser146=
ENST00000690993.1:n.515T>C
ENST00000691295.1:c.334-489T>C	ENSP00000508706.1:n.334-489T>C
ENST00000691918.1:c.417T>C	ENSP00000509525.1:p.Ser139=
ENST00000692152.1:c.369T>C	ENSP00000509317.1:p.Ser123=
ENST00000692344.1:n.462T>C
ENST00000693157.1:c.358T>C	ENSP00000510610.1:n.358T>C
ENST00000693363.1:c.438T>C	ENSP00000510411.1:p.Ser146=
ENST00000693367.1:c.438T>C	ENSP00000508815.1:p.Ser146=
ENST00000693639.1:c.431T>C	ENSP00000510223.1:p.Val144Ala
ENST00000693646.1:c.344T>C	ENSP00000508449.1:p.Val115Ala
ENST00000352397.10:c.438T>C MANE Select	ENSP00000338461.6:p.Ser146=
ENST00000352397.9:c.438T>C	ENSP00000338461.6:p.Ser146=
ENST00000361740.8:c.537T>C	ENSP00000354468.4:p.Ser179=
ENST00000402438.5:c.369T>C	ENSP00000385679.1:p.Ser123=
ENST00000407332.5:c.369T>C	ENSP00000384457.1:p.Ser123=
ENST00000407623.7:c.369T>C	ENSP00000384834.3:p.Ser123=
ENST00000438270.1:c.369T>C	ENSP00000403439.1:p.Ser123=
ENST00000470741.1:n.2572T>C
NM_000398.6:c.438T>C	NP_000389.1:p.Ser146=
NM_001129819.2:c.369T>C	NP_001123291.1:p.Ser123=
NM_001171660.1:c.537T>C	NP_001165131.1:p.Ser179=
NM_001171661.1:c.369T>C	NP_001165132.1:p.Ser123=
NM_007326.4:c.369T>C	NP_015565.1:p.Ser123=
NM_000398.7:c.438T>C MANE Select	NP_000389.1:p.Ser146=
NM_001171660.2:c.537T>C	NP_001165131.1:p.Ser179=