Canonical Allele Identifier: CA411797909

Gene: CYB5R3

Linked Data

• ClinVar Variation Id: 1502415
• ClinVar RCV Id: RCV002010977 ; RCV003485758
• dbSNP Id: rs1161477501
• gnomAD v2: 22-43023610-C-T
• gnomAD v3: 22-42627604-C-T
• gnomAD v4: 22-42627604-C-T
• MyVariant Identifiers: chr22:g.43023610C>T (hg19) ; chr22:g.42627604C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42627604C>T , CM000684.2:g.42627604C>T	GRCh38
NC_000022.10:g.43023610C>T , CM000684.1:g.43023610C>T	GRCh37
NC_000022.9:g.41353554C>T	NCBI36
NG_012194.1:g.26796G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361740.9:c.679+1G>A	ENSP00000354468.5:n.679+1G>A
ENST00000402438.6:c.478+1G>A	ENSP00000385679.1:n.478+1G>A
ENST00000407332.6:c.565+1G>A	ENSP00000384457.2:n.565+1G>A
ENST00000407623.8:c.478+1G>A	ENSP00000384834.3:n.478+1G>A
ENST00000617178.5:c.84+1G>A
ENST00000684963.1:n.2287+1G>A
ENST00000686523.1:c.*496+1G>A	ENSP00000508940.1:n.*496+1G>A
ENST00000687183.1:n.609G>A
ENST00000687198.1:c.478+1G>A	ENSP00000508492.1:n.478+1G>A
ENST00000688117.1:c.646+1G>A	ENSP00000509015.1:n.646+1G>A
ENST00000688244.1:c.333+3278G>A	ENSP00000510355.1:n.333+3278G>A
ENST00000689001.1:n.955G>A
ENST00000689195.1:c.464-215G>A	ENSP00000509895.1:n.464-215G>A
ENST00000689239.1:n.714+1G>A
ENST00000689795.1:n.709+1G>A
ENST00000690835.1:c.547+1G>A	ENSP00000509038.1:n.547+1G>A
ENST00000690993.1:n.1088G>A
ENST00000691295.1:c.*30+1G>A	ENSP00000508706.1:n.*30+1G>A
ENST00000691918.1:c.526+1G>A	ENSP00000509525.1:n.526+1G>A
ENST00000692152.1:c.478+1G>A	ENSP00000509317.1:n.478+1G>A
ENST00000692344.1:n.1034+1G>A
ENST00000693363.1:c.547+1G>A	ENSP00000510411.1:n.547+1G>A
ENST00000693367.1:c.547+1G>A	ENSP00000508815.1:n.547+1G>A
ENST00000693639.1:c.540+1G>A	ENSP00000510223.1:n.540+1G>A
ENST00000693646.1:c.453+1G>A	ENSP00000508449.1:n.453+1G>A
ENST00000352397.10:c.547+1G>A MANE Select	ENSP00000338461.6:n.547+1G>A
ENST00000352397.9:c.547+1G>A	ENSP00000338461.6:n.547+1G>A
ENST00000361740.8:c.646+1G>A	ENSP00000354468.4:n.646+1G>A
ENST00000402438.5:c.478+1G>A	ENSP00000385679.1:n.478+1G>A
ENST00000407332.5:c.478+1G>A	ENSP00000384457.1:n.478+1G>A
ENST00000407623.7:c.478+1G>A	ENSP00000384834.3:n.478+1G>A
ENST00000470741.1:n.2681+1G>A
NM_000398.6:c.547+1G>A	NP_000389.1:n.547+1G>A
NM_001129819.2:c.478+1G>A	NP_001123291.1:n.478+1G>A
NM_001171660.1:c.646+1G>A	NP_001165131.1:n.646+1G>A
NM_001171661.1:c.478+1G>A	NP_001165132.1:n.478+1G>A
NM_007326.4:c.478+1G>A	NP_015565.1:n.478+1G>A
NM_000398.7:c.547+1G>A MANE Select	NP_000389.1:n.547+1G>A
NM_001171660.2:c.646+1G>A	NP_001165131.1:n.646+1G>A