Canonical Allele Identifier: CA411798927

Gene: CYB5R3

Linked Data

• MyVariant Identifiers: chr22:g.43024163C>A (hg19) ; chr22:g.42628157C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42628157C>A , CM000684.2:g.42628157C>A	GRCh38
NC_000022.10:g.43024163C>A , CM000684.1:g.43024163C>A	GRCh37
NC_000022.9:g.41354107C>A	NCBI36
NG_012194.1:g.26243G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.458G>T	ENSP00000354468.5:p.Gly153Val
ENST00000402438.6:c.389G>T	ENSP00000385679.1:p.Gly130Val
ENST00000407332.6:c.476G>T	ENSP00000384457.2:p.Gly159Val
ENST00000407623.8:c.389G>T	ENSP00000384834.3:p.Gly130Val
ENST00000438270.2:c.389G>T	ENSP00000403439.2:p.Gly130Val
ENST00000684963.1:n.1735G>T
ENST00000686129.1:c.389G>T	ENSP00000508623.1:p.Gly130Val
ENST00000686523.1:c.*407G>T	ENSP00000508940.1:n.*407G>T
ENST00000687183.1:n.519G>T
ENST00000687198.1:c.389G>T	ENSP00000508492.1:p.Gly130Val
ENST00000688117.1:c.557G>T	ENSP00000509015.1:p.Gly186Val
ENST00000688244.1:c.333+2725G>T	ENSP00000510355.1:n.333+2725G>T
ENST00000689001.1:n.865G>T
ENST00000689195.1:c.458G>T	ENSP00000509895.1:p.Gly153Val
ENST00000689239.1:n.625G>T
ENST00000689795.1:n.620G>T
ENST00000690835.1:c.458G>T	ENSP00000509038.1:p.Gly153Val
ENST00000690993.1:n.535G>T
ENST00000691295.1:c.334-469G>T	ENSP00000508706.1:n.334-469G>T
ENST00000691918.1:c.437G>T	ENSP00000509525.1:p.Gly146Val
ENST00000692152.1:c.389G>T	ENSP00000509317.1:p.Gly130Val
ENST00000692344.1:n.482G>T
ENST00000693157.1:c.378G>T	ENSP00000510610.1:n.378G>T
ENST00000693363.1:c.458G>T	ENSP00000510411.1:p.Gly153Val
ENST00000693367.1:c.458G>T	ENSP00000508815.1:p.Gly153Val
ENST00000693639.1:c.451G>T	ENSP00000510223.1:p.Ala151Ser
ENST00000693646.1:c.364G>T	ENSP00000508449.1:p.Ala122Ser
ENST00000352397.10:c.458G>T MANE Select	ENSP00000338461.6:p.Gly153Val
ENST00000352397.9:c.458G>T	ENSP00000338461.6:p.Gly153Val
ENST00000361740.8:c.557G>T	ENSP00000354468.4:p.Gly186Val
ENST00000402438.5:c.389G>T	ENSP00000385679.1:p.Gly130Val
ENST00000407332.5:c.389G>T	ENSP00000384457.1:p.Gly130Val
ENST00000407623.7:c.389G>T	ENSP00000384834.3:p.Gly130Val
ENST00000438270.1:c.389G>T	ENSP00000403439.1:p.Gly130Val
ENST00000470741.1:n.2592G>T
NM_000398.6:c.458G>T	NP_000389.1:p.Gly153Val
NM_001129819.2:c.389G>T	NP_001123291.1:p.Gly130Val
NM_001171660.1:c.557G>T	NP_001165131.1:p.Gly186Val
NM_001171661.1:c.389G>T	NP_001165132.1:p.Gly130Val
NM_007326.4:c.389G>T	NP_015565.1:p.Gly130Val
NM_000398.7:c.458G>T MANE Select	NP_000389.1:p.Gly153Val
NM_001171660.2:c.557G>T	NP_001165131.1:p.Gly186Val