Canonical Allele Identifier: CA324695962

Gene: CYB5R3

Linked Data

• dbSNP Id: rs763610339
• MyVariant Identifiers: chr22:g.43020057_43020059del (hg19) ; chr22:g.42624051_42624053del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42624051_42624053del , CM000684.2:g.42624051_42624053del	GRCh38
NC_000022.10:g.43020057_43020059del , CM000684.1:g.43020057_43020059del	GRCh37
NC_000022.9:g.41350001_41350003del	NCBI36
NG_012194.1:g.30347_30349del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.766-165_766-163del	ENSP00000354468.5:n.766-165_766-163del
ENST00000402438.6:c.565-165_565-163del	ENSP00000385679.1:n.565-165_565-163del
ENST00000407332.6:c.652-165_652-163del	ENSP00000384457.2:n.652-165_652-163del
ENST00000407623.8:c.565-165_565-163del	ENSP00000384834.3:n.565-165_565-163del
ENST00000617178.5:c.171-165_171-163del
ENST00000684963.1:n.2374-165_2374-163del
ENST00000685184.1:n.61_63del
ENST00000686523.1:c.*583-165_*583-163del	ENSP00000508940.1:n.*583-165_*583-163del
ENST00000687183.1:n.910-165_910-163del
ENST00000687198.1:c.565-165_565-163del	ENSP00000508492.1:n.565-165_565-163del
ENST00000688117.1:c.733-165_733-163del	ENSP00000509015.1:n.733-165_733-163del
ENST00000688244.1:c.334-165_334-163del	ENSP00000510355.1:n.334-165_334-163del
ENST00000689001.1:n.1256-165_1256-163del
ENST00000689195.1:c.550-165_550-163del	ENSP00000509895.1:n.550-165_550-163del
ENST00000689239.1:n.801-165_801-163del
ENST00000689795.1:n.895-165_895-163del
ENST00000690835.1:c.*13-165_*13-163del	ENSP00000509038.1:n.*13-165_*13-163del
ENST00000690993.1:n.1389-165_1389-163del
ENST00000691295.1:c.*117-165_*117-163del	ENSP00000508706.1:n.*117-165_*117-163del
ENST00000691918.1:c.924-165_924-163del	ENSP00000509525.1:n.924-165_924-163del
ENST00000692152.1:c.565-165_565-163del	ENSP00000509317.1:n.565-165_565-163del
ENST00000692344.1:n.1121-165_1121-163del
ENST00000693363.1:c.676-165_676-163del	ENSP00000510411.1:n.676-165_676-163del
ENST00000693367.1:c.634-165_634-163del	ENSP00000508815.1:n.634-165_634-163del
ENST00000693639.1:c.627-165_627-163del	ENSP00000510223.1:n.627-165_627-163del
ENST00000693646.1:c.540-165_540-163del	ENSP00000508449.1:n.540-165_540-163del
ENST00000352397.10:c.634-165_634-163del MANE Select	ENSP00000338461.6:n.634-165_634-163del
ENST00000352397.9:c.634-165_634-163del	ENSP00000338461.6:n.634-165_634-163del
ENST00000361740.8:c.733-165_733-163del	ENSP00000354468.4:n.733-165_733-163del
ENST00000402438.5:c.565-165_565-163del	ENSP00000385679.1:n.565-165_565-163del
ENST00000407332.5:c.565-165_565-163del	ENSP00000384457.1:n.565-165_565-163del
ENST00000407623.7:c.565-165_565-163del	ENSP00000384834.3:n.565-165_565-163del
ENST00000470741.1:n.2768-165_2768-163del
NM_000398.6:c.634-165_634-163del	NP_000389.1:n.634-165_634-163del
NM_001129819.2:c.565-165_565-163del	NP_001123291.1:n.565-165_565-163del
NM_001171660.1:c.733-165_733-163del	NP_001165131.1:n.733-165_733-163del
NM_001171661.1:c.565-165_565-163del	NP_001165132.1:n.565-165_565-163del
NM_007326.4:c.565-165_565-163del	NP_015565.1:n.565-165_565-163del
NM_000398.7:c.634-165_634-163del MANE Select	NP_000389.1:n.634-165_634-163del
NM_001171660.2:c.733-165_733-163del	NP_001165131.1:n.733-165_733-163del