Canonical Allele Identifier: CA411800336
Gene: CYB5R3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42630900G>C , CM000684.2:g.42630900G>C GRCh38
NC_000022.10:g.43026906G>C , CM000684.1:g.43026906G>C GRCh37
NC_000022.9:g.41356850G>C NCBI36
NG_012194.1:g.23500C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361740.9:c.315C>G ENSP00000354468.5:p.Phe105Leu
ENST00000402438.6:c.246C>G ENSP00000385679.1:p.Phe82Leu
ENST00000407332.6:c.333C>G ENSP00000384457.2:p.Phe111Leu
ENST00000407623.8:c.246C>G ENSP00000384834.3:p.Phe82Leu
ENST00000438270.2:c.246C>G ENSP00000403439.2:p.Phe82Leu
ENST00000466276.2:n.382C>G
ENST00000686129.1:c.246C>G ENSP00000508623.1:p.Phe82Leu
ENST00000686523.1:c.*264C>G ENSP00000508940.1:n.*264C>G
ENST00000687183.1:n.376C>G
ENST00000687198.1:c.246C>G ENSP00000508492.1:p.Phe82Leu
ENST00000688117.1:c.414C>G ENSP00000509015.1:p.Phe138Leu
ENST00000688244.1:c.315C>G ENSP00000510355.1:p.Phe105Leu
ENST00000689001.1:n.722C>G
ENST00000689195.1:c.315C>G ENSP00000509895.1:p.Phe105Leu
ENST00000689239.1:n.482C>G
ENST00000689795.1:n.477C>G
ENST00000690835.1:c.315C>G ENSP00000509038.1:p.Phe105Leu
ENST00000690993.1:n.392C>G
ENST00000691295.1:c.315C>G ENSP00000508706.1:p.Phe105Leu
ENST00000691918.1:c.294C>G ENSP00000509525.1:p.Phe98Leu
ENST00000692152.1:c.246C>G ENSP00000509317.1:p.Phe82Leu
ENST00000692344.1:n.339C>G
ENST00000693157.1:c.235C>G ENSP00000510610.1:n.235C>G
ENST00000693363.1:c.315C>G ENSP00000510411.1:p.Phe105Leu
ENST00000693367.1:c.315C>G ENSP00000508815.1:p.Phe105Leu
ENST00000693639.1:c.308C>G ENSP00000510223.1:p.Ser103Trp
ENST00000693646.1:c.221C>G ENSP00000508449.1:p.Ser74Trp
ENST00000693716.1:n.543C>G
ENST00000352397.10:c.315C>G MANE Select ENSP00000338461.6:p.Phe105Leu
ENST00000352397.9:c.315C>G ENSP00000338461.6:p.Phe105Leu
ENST00000361740.8:c.414C>G ENSP00000354468.4:p.Phe138Leu
ENST00000402438.5:c.246C>G ENSP00000385679.1:p.Phe82Leu
ENST00000407332.5:c.246C>G ENSP00000384457.1:p.Phe82Leu
ENST00000407623.7:c.246C>G ENSP00000384834.3:p.Phe82Leu
ENST00000438270.1:c.246C>G ENSP00000403439.1:p.Phe82Leu
ENST00000470741.1:n.2449C>G
NM_000398.6:c.315C>G NP_000389.1:p.Phe105Leu
NM_001129819.2:c.246C>G NP_001123291.1:p.Phe82Leu
NM_001171660.1:c.414C>G NP_001165131.1:p.Phe138Leu
NM_001171661.1:c.246C>G NP_001165132.1:p.Phe82Leu
NM_007326.4:c.246C>G NP_015565.1:p.Phe82Leu
NM_000398.7:c.315C>G MANE Select NP_000389.1:p.Phe105Leu
NM_001171660.2:c.414C>G NP_001165131.1:p.Phe138Leu