Canonical Allele Identifier: CA2842993438

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623757C>A , CM000684.2:g.42623757C>A	GRCh38
NC_000022.10:g.43019763C>A , CM000684.1:g.43019763C>A	GRCh37
NC_000022.9:g.41349707C>A	NCBI36
NG_012194.1:g.30643G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.865+32G>T	ENSP00000354468.5:n.865+32G>T
ENST00000402438.6:c.664+32G>T	ENSP00000385679.1:n.664+32G>T
ENST00000407332.6:c.751+32G>T	ENSP00000384457.2:n.751+32G>T
ENST00000407623.8:c.664+32G>T	ENSP00000384834.3:n.664+32G>T
ENST00000617178.5:c.270+32G>T
ENST00000684963.1:n.2473+32G>T
ENST00000685184.1:n.325+32G>T
ENST00000686523.1:c.*682+32G>T	ENSP00000508940.1:n.*682+32G>T
ENST00000687183.1:n.1009+32G>T
ENST00000687198.1:c.664+32G>T	ENSP00000508492.1:n.664+32G>T
ENST00000688117.1:c.832+32G>T	ENSP00000509015.1:n.832+32G>T
ENST00000688244.1:c.433+32G>T	ENSP00000510355.1:n.433+32G>T
ENST00000689001.1:n.1355+32G>T
ENST00000689195.1:c.649+32G>T	ENSP00000509895.1:n.649+32G>T
ENST00000689239.1:n.900+32G>T
ENST00000689795.1:n.994+32G>T
ENST00000690835.1:c.*112+32G>T	ENSP00000509038.1:n.*112+32G>T
ENST00000690993.1:n.1488+32G>T
ENST00000691295.1:c.*216+32G>T	ENSP00000508706.1:n.*216+32G>T
ENST00000692152.1:c.664+32G>T	ENSP00000509317.1:n.664+32G>T
ENST00000692344.1:n.1220+32G>T
ENST00000693363.1:c.775+32G>T	ENSP00000510411.1:n.775+32G>T
ENST00000693367.1:c.733+32G>T	ENSP00000508815.1:n.733+32G>T
ENST00000352397.10:c.733+32G>T MANE Select	ENSP00000338461.6:n.733+32G>T
ENST00000352397.9:c.733+32G>T	ENSP00000338461.6:n.733+32G>T
ENST00000361740.8:c.832+32G>T	ENSP00000354468.4:n.832+32G>T
ENST00000402438.5:c.664+32G>T	ENSP00000385679.1:n.664+32G>T
ENST00000407332.5:c.664+32G>T	ENSP00000384457.1:n.664+32G>T
ENST00000407623.7:c.664+32G>T	ENSP00000384834.3:n.664+32G>T
ENST00000470741.1:n.2867+32G>T
NM_000398.6:c.733+32G>T	NP_000389.1:n.733+32G>T
NM_001129819.2:c.664+32G>T	NP_001123291.1:n.664+32G>T
NM_001171660.1:c.832+32G>T	NP_001165131.1:n.832+32G>T
NM_001171661.1:c.664+32G>T	NP_001165132.1:n.664+32G>T
NM_007326.4:c.664+32G>T	NP_015565.1:n.664+32G>T
NM_000398.7:c.733+32G>T MANE Select	NP_000389.1:n.733+32G>T
NM_001171660.2:c.832+32G>T	NP_001165131.1:n.832+32G>T