Canonical Allele Identifier: CA2406839210

Gene: CYB5R3

Linked Data

• dbSNP Id: rs1569321135

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42631202C>T , CM000684.2:g.42631202C>T	GRCh38
NC_000022.10:g.43027208C>T , CM000684.1:g.43027208C>T	GRCh37
NC_000022.9:g.41357152C>T	NCBI36
NG_012194.1:g.23198G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.226+176G>A	ENSP00000354468.5:n.226+176G>A
ENST00000402438.6:c.157+176G>A	ENSP00000385679.1:n.157+176G>A
ENST00000407332.6:c.244+176G>A	ENSP00000384457.2:n.244+176G>A
ENST00000407623.8:c.157+176G>A	ENSP00000384834.3:n.157+176G>A
ENST00000438270.2:c.157+176G>A	ENSP00000403439.2:n.157+176G>A
ENST00000466276.2:n.293+176G>A
ENST00000686129.1:c.157+176G>A	ENSP00000508623.1:n.157+176G>A
ENST00000686523.1:c.*175+176G>A	ENSP00000508940.1:n.*175+176G>A
ENST00000687183.1:n.287+176G>A
ENST00000687198.1:c.157+176G>A	ENSP00000508492.1:n.157+176G>A
ENST00000688117.1:c.325+176G>A	ENSP00000509015.1:n.325+176G>A
ENST00000688244.1:c.226+176G>A	ENSP00000510355.1:n.226+176G>A
ENST00000689001.1:n.420G>A
ENST00000689195.1:c.226+176G>A	ENSP00000509895.1:n.226+176G>A
ENST00000689239.1:n.393+176G>A
ENST00000689795.1:n.388+176G>A
ENST00000690835.1:c.226+176G>A	ENSP00000509038.1:n.226+176G>A
ENST00000690993.1:n.303+176G>A
ENST00000691295.1:c.226+176G>A	ENSP00000508706.1:n.226+176G>A
ENST00000691918.1:c.205+176G>A	ENSP00000509525.1:n.205+176G>A
ENST00000692152.1:c.157+176G>A	ENSP00000509317.1:n.157+176G>A
ENST00000692344.1:n.250+176G>A
ENST00000693157.1:c.147-214G>A	ENSP00000510610.1:n.147-214G>A
ENST00000693363.1:c.226+176G>A	ENSP00000510411.1:n.226+176G>A
ENST00000693367.1:c.226+176G>A	ENSP00000508815.1:n.226+176G>A
ENST00000693639.1:c.219+176G>A	ENSP00000510223.1:n.219+176G>A
ENST00000693646.1:c.133-214G>A	ENSP00000508449.1:n.133-214G>A
ENST00000693716.1:n.454+176G>A
ENST00000352397.10:c.226+176G>A MANE Select	ENSP00000338461.6:n.226+176G>A
ENST00000352397.9:c.226+176G>A	ENSP00000338461.6:n.226+176G>A
ENST00000361740.8:c.325+176G>A	ENSP00000354468.4:n.325+176G>A
ENST00000402438.5:c.157+176G>A	ENSP00000385679.1:n.157+176G>A
ENST00000407332.5:c.157+176G>A	ENSP00000384457.1:n.157+176G>A
ENST00000407623.7:c.157+176G>A	ENSP00000384834.3:n.157+176G>A
ENST00000438270.1:c.157+176G>A	ENSP00000403439.1:n.157+176G>A
ENST00000466276.1:n.420G>A
ENST00000470741.1:n.2147G>A
NM_000398.6:c.226+176G>A	NP_000389.1:n.226+176G>A
NM_001129819.2:c.157+176G>A	NP_001123291.1:n.157+176G>A
NM_001171660.1:c.325+176G>A	NP_001165131.1:n.325+176G>A
NM_001171661.1:c.157+176G>A	NP_001165132.1:n.157+176G>A
NM_007326.4:c.157+176G>A	NP_015565.1:n.157+176G>A
NM_000398.7:c.226+176G>A MANE Select	NP_000389.1:n.226+176G>A
NM_001171660.2:c.325+176G>A	NP_001165131.1:n.325+176G>A