Canonical Allele Identifier: CA411796165

Gene: CYB5R3

Linked Data

• dbSNP Id: rs794728011
• MyVariant Identifiers: chr22:g.43015952C>T (hg19) ; chr22:g.42619946C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42619946C>T , CM000684.2:g.42619946C>T	GRCh38
NC_000022.10:g.43015952C>T , CM000684.1:g.43015952C>T	GRCh37
NC_000022.9:g.41345896C>T	NCBI36
NG_012194.1:g.34454G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361740.9:c.866-1G>A	ENSP00000354468.5:n.866-1G>A
ENST00000402438.6:c.665-1G>A	ENSP00000385679.1:n.665-1G>A
ENST00000407332.6:c.752-1G>A	ENSP00000384457.2:n.752-1G>A
ENST00000407623.8:c.665-1G>A	ENSP00000384834.3:n.665-1G>A
ENST00000617178.5:c.271-1G>A
ENST00000684963.1:n.2474-1G>A
ENST00000685184.1:n.326-1G>A
ENST00000686523.1:c.*683-1G>A	ENSP00000508940.1:n.*683-1G>A
ENST00000687183.1:n.1010-1G>A
ENST00000687198.1:c.665-1G>A	ENSP00000508492.1:n.665-1G>A
ENST00000688117.1:c.833-1G>A	ENSP00000509015.1:n.833-1G>A
ENST00000688244.1:c.434-1G>A	ENSP00000510355.1:n.434-1G>A
ENST00000689001.1:n.1356-1G>A
ENST00000689195.1:c.650-1G>A	ENSP00000509895.1:n.650-1G>A
ENST00000689239.1:n.901-1G>A
ENST00000689795.1:n.995-1G>A
ENST00000690835.1:c.*113-1G>A	ENSP00000509038.1:n.*113-1G>A
ENST00000690993.1:n.1489-1G>A
ENST00000691295.1:c.*217-1G>A	ENSP00000508706.1:n.*217-1G>A
ENST00000692152.1:c.665-1G>A	ENSP00000509317.1:n.665-1G>A
ENST00000692344.1:n.1221-1G>A
ENST00000693363.1:c.776-1G>A	ENSP00000510411.1:n.776-1G>A
ENST00000693367.1:c.734-1G>A	ENSP00000508815.1:n.734-1G>A
ENST00000352397.10:c.734-1G>A MANE Select	ENSP00000338461.6:n.734-1G>A
ENST00000352397.9:c.734-1G>A	ENSP00000338461.6:n.734-1G>A
ENST00000361740.8:c.833-1G>A	ENSP00000354468.4:n.833-1G>A
ENST00000402438.5:c.665-1G>A	ENSP00000385679.1:n.665-1G>A
ENST00000407332.5:c.665-1G>A	ENSP00000384457.1:n.665-1G>A
ENST00000407623.7:c.665-1G>A	ENSP00000384834.3:n.665-1G>A
ENST00000470741.1:n.2868-1G>A
NM_000398.6:c.734-1G>A	NP_000389.1:n.734-1G>A
NM_001129819.2:c.665-1G>A	NP_001123291.1:n.665-1G>A
NM_001171660.1:c.833-1G>A	NP_001165131.1:n.833-1G>A
NM_001171661.1:c.665-1G>A	NP_001165132.1:n.665-1G>A
NM_007326.4:c.665-1G>A	NP_015565.1:n.665-1G>A
NM_000398.7:c.734-1G>A MANE Select	NP_000389.1:n.734-1G>A
NM_001171660.2:c.833-1G>A	NP_001165131.1:n.833-1G>A