Canonical Allele Identifier: CA2657075538

Gene: CYB5R3

Linked Data

• gnomAD v4: 22-42624004-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42624004C>T , CM000684.2:g.42624004C>T	GRCh38
NC_000022.10:g.43020010C>T , CM000684.1:g.43020010C>T	GRCh37
NC_000022.9:g.41349954C>T	NCBI36
NG_012194.1:g.30396G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.766-116G>A	ENSP00000354468.5:n.766-116G>A
ENST00000402438.6:c.565-116G>A	ENSP00000385679.1:n.565-116G>A
ENST00000407332.6:c.652-116G>A	ENSP00000384457.2:n.652-116G>A
ENST00000407623.8:c.565-116G>A	ENSP00000384834.3:n.565-116G>A
ENST00000617178.5:c.171-116G>A
ENST00000684963.1:n.2374-116G>A
ENST00000685184.1:n.110G>A
ENST00000686523.1:c.*583-116G>A	ENSP00000508940.1:n.*583-116G>A
ENST00000687183.1:n.910-116G>A
ENST00000687198.1:c.565-116G>A	ENSP00000508492.1:n.565-116G>A
ENST00000688117.1:c.733-116G>A	ENSP00000509015.1:n.733-116G>A
ENST00000688244.1:c.334-116G>A	ENSP00000510355.1:n.334-116G>A
ENST00000689001.1:n.1256-116G>A
ENST00000689195.1:c.550-116G>A	ENSP00000509895.1:n.550-116G>A
ENST00000689239.1:n.801-116G>A
ENST00000689795.1:n.895-116G>A
ENST00000690835.1:c.*13-116G>A	ENSP00000509038.1:n.*13-116G>A
ENST00000690993.1:n.1389-116G>A
ENST00000691295.1:c.*117-116G>A	ENSP00000508706.1:n.*117-116G>A
ENST00000691918.1:c.924-116G>A	ENSP00000509525.1:n.924-116G>A
ENST00000692152.1:c.565-116G>A	ENSP00000509317.1:n.565-116G>A
ENST00000692344.1:n.1121-116G>A
ENST00000693363.1:c.676-116G>A	ENSP00000510411.1:n.676-116G>A
ENST00000693367.1:c.634-116G>A	ENSP00000508815.1:n.634-116G>A
ENST00000693639.1:c.627-116G>A	ENSP00000510223.1:n.627-116G>A
ENST00000693646.1:c.540-116G>A	ENSP00000508449.1:n.540-116G>A
ENST00000352397.10:c.634-116G>A MANE Select	ENSP00000338461.6:n.634-116G>A
ENST00000352397.9:c.634-116G>A	ENSP00000338461.6:n.634-116G>A
ENST00000361740.8:c.733-116G>A	ENSP00000354468.4:n.733-116G>A
ENST00000402438.5:c.565-116G>A	ENSP00000385679.1:n.565-116G>A
ENST00000407332.5:c.565-116G>A	ENSP00000384457.1:n.565-116G>A
ENST00000407623.7:c.565-116G>A	ENSP00000384834.3:n.565-116G>A
ENST00000470741.1:n.2768-116G>A
NM_000398.6:c.634-116G>A	NP_000389.1:n.634-116G>A
NM_001129819.2:c.565-116G>A	NP_001123291.1:n.565-116G>A
NM_001171660.1:c.733-116G>A	NP_001165131.1:n.733-116G>A
NM_001171661.1:c.565-116G>A	NP_001165132.1:n.565-116G>A
NM_007326.4:c.565-116G>A	NP_015565.1:n.565-116G>A
NM_000398.7:c.634-116G>A MANE Select	NP_000389.1:n.634-116G>A
NM_001171660.2:c.733-116G>A	NP_001165131.1:n.733-116G>A