Canonical Allele Identifier: CA2406837480

Gene: CYB5R3

Linked Data

• dbSNP Id: rs1928391418

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42628113_42628114insGGA , CM000684.2:g.42628113_42628114insGGA	GRCh38
NC_000022.10:g.43024119_43024120insGGA , CM000684.1:g.43024119_43024120insGGA	GRCh37
NC_000022.9:g.41354063_41354064insGGA	NCBI36
NG_012194.1:g.26286_26287insTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.463+38_463+39insTCC	ENSP00000354468.5:n.463+38_463+39insTCC
ENST00000402438.6:c.394+38_394+39insTCC	ENSP00000385679.1:n.394+38_394+39insTCC
ENST00000407332.6:c.481+38_481+39insTCC	ENSP00000384457.2:n.481+38_481+39insTCC
ENST00000407623.8:c.394+38_394+39insTCC	ENSP00000384834.3:n.394+38_394+39insTCC
ENST00000438270.2:c.394+38_394+39insTCC	ENSP00000403439.2:n.394+38_394+39insTCC
ENST00000684963.1:n.1778_1779insTCC
ENST00000686523.1:c.*412+38_*412+39insTCC	ENSP00000508940.1:n.*412+38_*412+39insTCC
ENST00000687183.1:n.524+38_524+39insTCC
ENST00000687198.1:c.394+38_394+39insTCC	ENSP00000508492.1:n.394+38_394+39insTCC
ENST00000688117.1:c.562+38_562+39insTCC	ENSP00000509015.1:n.562+38_562+39insTCC
ENST00000688244.1:c.333+2768_333+2769insTCC	ENSP00000510355.1:n.333+2768_333+2769insTCC
ENST00000689001.1:n.870+38_870+39insTCC
ENST00000689195.1:c.463+38_463+39insTCC	ENSP00000509895.1:n.463+38_463+39insTCC
ENST00000689239.1:n.630+38_630+39insTCC
ENST00000689795.1:n.625+38_625+39insTCC
ENST00000690835.1:c.463+38_463+39insTCC	ENSP00000509038.1:n.463+38_463+39insTCC
ENST00000690993.1:n.578_579insTCC
ENST00000691295.1:c.334-426_334-425insTCC	ENSP00000508706.1:n.334-426_334-425insTCC
ENST00000691918.1:c.442+38_442+39insTCC	ENSP00000509525.1:n.442+38_442+39insTCC
ENST00000692152.1:c.394+38_394+39insTCC	ENSP00000509317.1:n.394+38_394+39insTCC
ENST00000692344.1:n.525_526insTCC
ENST00000693363.1:c.463+38_463+39insTCC	ENSP00000510411.1:n.463+38_463+39insTCC
ENST00000693367.1:c.463+38_463+39insTCC	ENSP00000508815.1:n.463+38_463+39insTCC
ENST00000693639.1:c.456+38_456+39insTCC	ENSP00000510223.1:n.456+38_456+39insTCC
ENST00000693646.1:c.369+38_369+39insTCC	ENSP00000508449.1:n.369+38_369+39insTCC
ENST00000352397.10:c.463+38_463+39insTCC MANE Select	ENSP00000338461.6:n.463+38_463+39insTCC
ENST00000352397.9:c.463+38_463+39insTCC	ENSP00000338461.6:n.463+38_463+39insTCC
ENST00000361740.8:c.562+38_562+39insTCC	ENSP00000354468.4:n.562+38_562+39insTCC
ENST00000402438.5:c.394+38_394+39insTCC	ENSP00000385679.1:n.394+38_394+39insTCC
ENST00000407332.5:c.394+38_394+39insTCC	ENSP00000384457.1:n.394+38_394+39insTCC
ENST00000407623.7:c.394+38_394+39insTCC	ENSP00000384834.3:n.394+38_394+39insTCC
ENST00000438270.1:c.394+38_394+39insTCC	ENSP00000403439.1:n.394+38_394+39insTCC
ENST00000470741.1:n.2597+38_2597+39insTCC
NM_000398.6:c.463+38_463+39insTCC	NP_000389.1:n.463+38_463+39insTCC
NM_001129819.2:c.394+38_394+39insTCC	NP_001123291.1:n.394+38_394+39insTCC
NM_001171660.1:c.562+38_562+39insTCC	NP_001165131.1:n.562+38_562+39insTCC
NM_001171661.1:c.394+38_394+39insTCC	NP_001165132.1:n.394+38_394+39insTCC
NM_007326.4:c.394+38_394+39insTCC	NP_015565.1:n.394+38_394+39insTCC
NM_000398.7:c.463+38_463+39insTCC MANE Select	NP_000389.1:n.463+38_463+39insTCC
NM_001171660.2:c.562+38_562+39insTCC	NP_001165131.1:n.562+38_562+39insTCC