Canonical Allele Identifier: CA411798585

Gene: CYB5R3

Linked Data

• gnomAD v4: 22-42627688-C-A
• MyVariant Identifiers: chr22:g.43023694C>A (hg19) ; chr22:g.42627688C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42627688C>A , CM000684.2:g.42627688C>A	GRCh38
NC_000022.10:g.43023694C>A , CM000684.1:g.43023694C>A	GRCh37
NC_000022.9:g.41353638C>A	NCBI36
NG_012194.1:g.26712G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.596G>T	ENSP00000354468.5:p.Gly199Val
ENST00000402438.6:c.395G>T	ENSP00000385679.1:p.Gly132Val
ENST00000407332.6:c.482G>T	ENSP00000384457.2:p.Gly161Val
ENST00000407623.8:c.395G>T	ENSP00000384834.3:p.Gly132Val
ENST00000438270.2:c.395G>T	ENSP00000403439.2:p.Gly132Val
ENST00000617178.5:c.1G>T
ENST00000684963.1:n.2204G>T
ENST00000686523.1:c.*413G>T	ENSP00000508940.1:n.*413G>T
ENST00000687183.1:n.525G>T
ENST00000687198.1:c.395G>T	ENSP00000508492.1:p.Gly132Val
ENST00000688117.1:c.563G>T	ENSP00000509015.1:p.Gly188Val
ENST00000688244.1:c.333+3194G>T	ENSP00000510355.1:n.333+3194G>T
ENST00000689001.1:n.871G>T
ENST00000689195.1:c.464-299G>T	ENSP00000509895.1:n.464-299G>T
ENST00000689239.1:n.631G>T
ENST00000689795.1:n.626G>T
ENST00000690835.1:c.464G>T	ENSP00000509038.1:p.Gly155Val
ENST00000690993.1:n.1004G>T
ENST00000691295.1:c.334G>T	ENSP00000508706.1:p.Gly112Ter
ENST00000691918.1:c.443G>T	ENSP00000509525.1:p.Gly148Val
ENST00000692152.1:c.395G>T	ENSP00000509317.1:p.Gly132Val
ENST00000692344.1:n.951G>T
ENST00000693363.1:c.464G>T	ENSP00000510411.1:p.Gly155Val
ENST00000693367.1:c.464G>T	ENSP00000508815.1:p.Gly155Val
ENST00000693639.1:c.457G>T	ENSP00000510223.1:p.Gly153Ter
ENST00000693646.1:c.370G>T	ENSP00000508449.1:p.Gly124Ter
ENST00000352397.10:c.464G>T MANE Select	ENSP00000338461.6:p.Gly155Val
ENST00000352397.9:c.464G>T	ENSP00000338461.6:p.Gly155Val
ENST00000361740.8:c.563G>T	ENSP00000354468.4:p.Gly188Val
ENST00000402438.5:c.395G>T	ENSP00000385679.1:p.Gly132Val
ENST00000407332.5:c.395G>T	ENSP00000384457.1:p.Gly132Val
ENST00000407623.7:c.395G>T	ENSP00000384834.3:p.Gly132Val
ENST00000438270.1:c.395G>T	ENSP00000403439.1:p.Gly132Val
ENST00000470741.1:n.2598G>T
NM_000398.6:c.464G>T	NP_000389.1:p.Gly155Val
NM_001129819.2:c.395G>T	NP_001123291.1:p.Gly132Val
NM_001171660.1:c.563G>T	NP_001165131.1:p.Gly188Val
NM_001171661.1:c.395G>T	NP_001165132.1:p.Gly132Val
NM_007326.4:c.395G>T	NP_015565.1:p.Gly132Val
NM_000398.7:c.464G>T MANE Select	NP_000389.1:p.Gly155Val
NM_001171660.2:c.563G>T	NP_001165131.1:p.Gly188Val