Canonical Allele Identifier: CA10269592

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42619953G>A , CM000684.2:g.42619953G>A	GRCh38
NC_000022.10:g.43015959G>A , CM000684.1:g.43015959G>A	GRCh37
NC_000022.9:g.41345903G>A	NCBI36
NG_012194.1:g.34447C>T

Transcript Alleles

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